26 Hematology jobs in Canada
Global Study Manager (Hematology/Oncology)
ICON Clinical Research
Posted today
Job Viewed
Job Description
Global Study Manager (hematology/oncology)
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
**What you will be doing:**
- Contribute to the development of study documents as appropriate as well as any updates/amendments, ensuring template and version compliance.
- Lead the preparation of country specific agreements, confidentiality agreements, clinical trial applications and other applicable country documents.
- Manage the set-up of third-party vendors assessing initial statement of work and budget, as well as the change order process.
- Provide input to data management documents (e.g. Case Report Form, Data Validation Specifications), and interface with data management representatives and sites to facilitate the delivery of study data.
- Initiate contract/budget requests and track ongoing status; facilitate generation of purchase orders, review vendor invoices and assist in tracking spend against approved budget.
- Ensure the supply of Investigational product and study materials by liaising with Drug Supply or external service providers as appropriate.
- Oversight of third party vendors, global / local internal staff and investigator sites to support effective delivery of a study and its regulatory documents from development of the protocol through to the Clinical Study Report.
- Provide oversight of and support recruitment and data delivery as well as risk mitigation strategies.
- Assist in the clinical trial insurance process; track approvals, revisions and renewals of certificates.
- Monitor study conduct and progress, proactively identifying and resolving issues which may impact delivery of the study to the necessary quality, timelines or budget.
- Support risk management and quality efforts to ensure study compliance.
- Support set-up, maintenance, closeout and archiving of the Trial Master File (TMF), ensuring continual inspection readiness.
- Prepare presentation material for meetings, newsletters and websites.
- Support the study team in the implementation of audits and regulatory inspections.
- Contribute to review of new/amended/unique SOPs and guidance documents.
Your Profile
- University degree / Bachelor's degree, preferably in medical or biological science, or discipline associated with Clinical Research, or equivalent experience
- Minimum of 3 years clinical trial management experience
- Experience of working with and delivering through strategic partners and 3rd party vendors
- Experience in oncology/hematology (blood cancers)
- Experience working on a global level
- Candidate must reside in Eastern Canada - limited travel may be required
- Experience in external provider oversight and management
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
**What you will be doing:**
- Contribute to the development of study documents as appropriate as well as any updates/amendments, ensuring template and version compliance.
- Lead the preparation of country specific agreements, confidentiality agreements, clinical trial applications and other applicable country documents.
- Manage the set-up of third-party vendors assessing initial statement of work and budget, as well as the change order process.
- Provide input to data management documents (e.g. Case Report Form, Data Validation Specifications), and interface with data management representatives and sites to facilitate the delivery of study data.
- Initiate contract/budget requests and track ongoing status; facilitate generation of purchase orders, review vendor invoices and assist in tracking spend against approved budget.
- Ensure the supply of Investigational product and study materials by liaising with Drug Supply or external service providers as appropriate.
- Oversight of third party vendors, global / local internal staff and investigator sites to support effective delivery of a study and its regulatory documents from development of the protocol through to the Clinical Study Report.
- Provide oversight of and support recruitment and data delivery as well as risk mitigation strategies.
- Assist in the clinical trial insurance process; track approvals, revisions and renewals of certificates.
- Monitor study conduct and progress, proactively identifying and resolving issues which may impact delivery of the study to the necessary quality, timelines or budget.
- Support risk management and quality efforts to ensure study compliance.
- Support set-up, maintenance, closeout and archiving of the Trial Master File (TMF), ensuring continual inspection readiness.
- Prepare presentation material for meetings, newsletters and websites.
- Support the study team in the implementation of audits and regulatory inspections.
- Contribute to review of new/amended/unique SOPs and guidance documents.
Your Profile
- University degree / Bachelor's degree, preferably in medical or biological science, or discipline associated with Clinical Research, or equivalent experience
- Minimum of 3 years clinical trial management experience
- Experience of working with and delivering through strategic partners and 3rd party vendors
- Experience in oncology/hematology (blood cancers)
- Experience working on a global level
- Candidate must reside in Eastern Canada - limited travel may be required
- Experience in external provider oversight and management
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
This advertiser has chosen not to accept applicants from your region.
0
Director Medical Affairs Hematology - Canada
Mississauga, Ontario
Regeneron Pharmaceuticals
Posted 3 days ago
Job Viewed
Job Description
**Medical Affairs Director, Hematology**
**Regeneron Canada - Toronto**
At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we're establishing new ways to think about science, manufacturing and commercialization.
Our **Medical Directors in Hematology** play a pivotal role as professionals with Hematology expertise and scientific knowledge. They deliver strategic and operational leadership by thoroughly understanding the therapeutic area and serving as a key medical resource to medical specialists, healthcare professionals, payers, and internal collaborators.
We are looking for our next team member to join our passionate & dedicated Medical Affairs team in Toronto.
**Medical Affairs Director, Hematology**
**Toronto, Canada**
The Medical Director Hematology represents Regeneron in its Medical Affairs and Clinical Development functions in country. The incumbent provides scientific and medical leadership by thoroughly understanding the assigned Hematology assets and serving as a key medical resource.
Working in a multifunctional, matrix organization with Global and US teams, the Medical Director Hematology is responsible for strategic medical operations in Hematology in the country. The Medical Director Hematology aligns with the Country Medical Director and ensures that such medical and clinical activities in country are aligned with overarching global strategies, goals and operations.
You will work in a **multifunctional, matrix organization** within the medical affairs group, as well as with colleagues in clinical development, operations, regulatory, commercial, access & reimbursement, and patient advocacy. You will also collaborate with external partners such as healthcare practitioners, research groups, payers, and alliance partners.
**In this role, a typical day may include the following:**
+ **Scientific engagement** with external communities to educate and advance scientific and medical understanding of Hematology disease areas, including the management of disease, standards of patient care, and roles of our medicines.
+ **Building strong working relationships** with external partners, including patient groups and professional organizations.
+ Continuously maintaining **deep scientific and medical knowledge** in Hematology, as well as a deep understanding of patient and physician interactions and clinical decision-making.
+ **Representing Regeneron** in scientific engagement with external communities to advance understanding of our medicines, disease management, and patient care.
+ Proactively bringing **patients' and physicians' voices** from a local perspective to cross-functional teams to ensure that Regeneron medicines meet their needs, while considering external stakeholders.
+ **Acting as an effective Regeneron representative** by interacting with external experts and attending professional/medical meetings as the in-country representative for Hematology products.
+ Collaborating to create the **medical strategy** and executing it with appropriate content for congresses, symposia, and advisory boards, facilitating and executing such activities in Canada.
+ Delivering **scientific presentations** to diverse audiences (e.g., physicians, pharmacists, nurses, payers, agencies, and other key stakeholders) in various meetings and activities.
+ Providing **medical guidance and support** to the local clinical research 'field operational' teams where appropriate.
+ Assessing **medical education needs** in Canada and executing internal and external educational strategies as needed.
+ Providing **medical input** into commercialization strategies in Canada while maintaining scientific integrity and serving as the local medical representative on global teams.
+ Supporting the development and execution of an **integrated strategy** for optimal country readiness and life cycle management initiatives.
+ Ensuring scientific review of **local promotional materials, medical materials, and publications** in compliance with Canadian regulations.
+ Establishing a highly functioning, patient-centric, credible and compliant medical organization in Hematology, responsible for the management of a Hematology Medical team
**This role may be for you if:**
+ You have an **outstanding work ethic and integrity** , including high ethical and scientific standards.
+ You are able to work effectively in a **fast-paced, rapidly changing environment** , and cooperatively across the organization to achieve shared objectives.
+ You enjoy bringing **new and unique ideas** that move science forward and are comfortable dealing with scientific concepts and complexity.
+ You have the ability to make **sound decisions** based on analysis, wisdom, experience, and judgment, even under tight deadlines and pressure.
+ You possess **strong motivational, negotiation, listening, and analytic skills** and can work independently while engaging in collaborative decision-making.
+ You are comfortable with **change, uncertainty, and risk** , and can shift gears comfortably while acting without having the total picture.
+ You have strong leadership and management skills, with an ability to foster inclusion, to develop and coach others, to inspire and motivate others, to promote collaboration with an entrepreneurial mindset.
**To be considered for this role, you must have:**
+ **M.D., PhD, or PharmD** with expertise in **Hematology** disease areas.
+ A minimum of **10 years of experience** in the pharmaceutical industry and/or medical affairs, with clinical, research, or drug-development experience in Hematology.
+ Successfully working in a matrix, cross-functional environment; excellent collaboration skills; experience working across functions to achieve results.
+ Excellent medical communication skills and a thorough understanding of the healthcare environment, including external partners.
+ Disease area expertise and medical and/or clinical experience, with demonstrated understanding of medical affairs accountabilities for evidence generation, external engagement, and internal advice.
+ Ability and willingness to travel up to 30% of the time.
+ Proficiency in both English and French (spoken and written) is a valuable asset.
If you are passionate about advancing Hematology care and making a difference in patients' lives, we encourage you to apply!
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
**Regeneron Canada - Toronto**
At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we're establishing new ways to think about science, manufacturing and commercialization.
Our **Medical Directors in Hematology** play a pivotal role as professionals with Hematology expertise and scientific knowledge. They deliver strategic and operational leadership by thoroughly understanding the therapeutic area and serving as a key medical resource to medical specialists, healthcare professionals, payers, and internal collaborators.
We are looking for our next team member to join our passionate & dedicated Medical Affairs team in Toronto.
**Medical Affairs Director, Hematology**
**Toronto, Canada**
The Medical Director Hematology represents Regeneron in its Medical Affairs and Clinical Development functions in country. The incumbent provides scientific and medical leadership by thoroughly understanding the assigned Hematology assets and serving as a key medical resource.
Working in a multifunctional, matrix organization with Global and US teams, the Medical Director Hematology is responsible for strategic medical operations in Hematology in the country. The Medical Director Hematology aligns with the Country Medical Director and ensures that such medical and clinical activities in country are aligned with overarching global strategies, goals and operations.
You will work in a **multifunctional, matrix organization** within the medical affairs group, as well as with colleagues in clinical development, operations, regulatory, commercial, access & reimbursement, and patient advocacy. You will also collaborate with external partners such as healthcare practitioners, research groups, payers, and alliance partners.
**In this role, a typical day may include the following:**
+ **Scientific engagement** with external communities to educate and advance scientific and medical understanding of Hematology disease areas, including the management of disease, standards of patient care, and roles of our medicines.
+ **Building strong working relationships** with external partners, including patient groups and professional organizations.
+ Continuously maintaining **deep scientific and medical knowledge** in Hematology, as well as a deep understanding of patient and physician interactions and clinical decision-making.
+ **Representing Regeneron** in scientific engagement with external communities to advance understanding of our medicines, disease management, and patient care.
+ Proactively bringing **patients' and physicians' voices** from a local perspective to cross-functional teams to ensure that Regeneron medicines meet their needs, while considering external stakeholders.
+ **Acting as an effective Regeneron representative** by interacting with external experts and attending professional/medical meetings as the in-country representative for Hematology products.
+ Collaborating to create the **medical strategy** and executing it with appropriate content for congresses, symposia, and advisory boards, facilitating and executing such activities in Canada.
+ Delivering **scientific presentations** to diverse audiences (e.g., physicians, pharmacists, nurses, payers, agencies, and other key stakeholders) in various meetings and activities.
+ Providing **medical guidance and support** to the local clinical research 'field operational' teams where appropriate.
+ Assessing **medical education needs** in Canada and executing internal and external educational strategies as needed.
+ Providing **medical input** into commercialization strategies in Canada while maintaining scientific integrity and serving as the local medical representative on global teams.
+ Supporting the development and execution of an **integrated strategy** for optimal country readiness and life cycle management initiatives.
+ Ensuring scientific review of **local promotional materials, medical materials, and publications** in compliance with Canadian regulations.
+ Establishing a highly functioning, patient-centric, credible and compliant medical organization in Hematology, responsible for the management of a Hematology Medical team
**This role may be for you if:**
+ You have an **outstanding work ethic and integrity** , including high ethical and scientific standards.
+ You are able to work effectively in a **fast-paced, rapidly changing environment** , and cooperatively across the organization to achieve shared objectives.
+ You enjoy bringing **new and unique ideas** that move science forward and are comfortable dealing with scientific concepts and complexity.
+ You have the ability to make **sound decisions** based on analysis, wisdom, experience, and judgment, even under tight deadlines and pressure.
+ You possess **strong motivational, negotiation, listening, and analytic skills** and can work independently while engaging in collaborative decision-making.
+ You are comfortable with **change, uncertainty, and risk** , and can shift gears comfortably while acting without having the total picture.
+ You have strong leadership and management skills, with an ability to foster inclusion, to develop and coach others, to inspire and motivate others, to promote collaboration with an entrepreneurial mindset.
**To be considered for this role, you must have:**
+ **M.D., PhD, or PharmD** with expertise in **Hematology** disease areas.
+ A minimum of **10 years of experience** in the pharmaceutical industry and/or medical affairs, with clinical, research, or drug-development experience in Hematology.
+ Successfully working in a matrix, cross-functional environment; excellent collaboration skills; experience working across functions to achieve results.
+ Excellent medical communication skills and a thorough understanding of the healthcare environment, including external partners.
+ Disease area expertise and medical and/or clinical experience, with demonstrated understanding of medical affairs accountabilities for evidence generation, external engagement, and internal advice.
+ Ability and willingness to travel up to 30% of the time.
+ Proficiency in both English and French (spoken and written) is a valuable asset.
If you are passionate about advancing Hematology care and making a difference in patients' lives, we encourage you to apply!
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
This advertiser has chosen not to accept applicants from your region.
1
Hematology/Oncology Physician - Per Diem
Surrey, British Columbia
PeaceHealth
Posted 21 days ago
Job Viewed
Job Description
**Description**
PeaceHealth is seeking a Hematology/Oncology physician who could provide per diem coverage based in beautiful Sedro-Woolley, Washington located half-way between Seattle and Vancouver, British Columbia.
Unique opportunity to be part of a larger oncology team in a beautiful, growing community where patients value their physicians and health caregivers. The ideal candidate will be Board Certified.
Why you'll love the practice
+ The cancer center at United General Medical Center (UGMC) has a hub & spoke model with PeaceHealth St. Joseph Cancer Center in Bellingham, WA
+ Full range of services in one location: Medical Oncology and Radiation Oncology, 24/7 emergency contact line, RapidArc radio therapy and SBRT, 9 infusion chairs, resource center with boutique for patients, designated patient navigators
+ Commission on Cancer Accreditation responsibilities
+ Strong primary and specialty care presence in Sedro-Woolley/Burlington area
+ Epic EMR
Position is paid at $282.66/hour and includes medical malpractice coverage with tail coverage. Potential for travel/accommodation stipend and license reimbursement.
**Please reach out to learn more: Manjit Kaur, Physician and Clinician Recruiter;** ** **
Sedro-Woolley, WA, the "Gateway to the North Cascades," is a wonderful blend of incredible scenery, endless outdoor recreation and small-town living! Stroll through historic downtown to see life-size chainsaw art sculptures carved from cedar logs at the annual Loggerodeo. The seasonal Farmers Market offers some of Skagit County's freshest produce, meats, cheeses, flowers, handcrafted goods and snacks, and Riverfront Park offers picnicking and boating beside the Skagit River. There are unlimited opportunities for breathtaking hikes, relaxing camping trips, water activities, bird watching, snow sports, scenic drives and horseback riding. Both Sedro-Woolley and neighboring Burlington, WA (known as "The Hub of Skagit County") offer many Arts, Culture, Entertainment and retail opportunities, including the famous Skagit Tulip Festival. Finally, if you want to visit a bigger city, Sedro-Woolley is a quick 20-minute drive to Bellingham, a 90-minute drive to Seattle, WA and a 90-minute drive to Vancouver, British Columbia.
_A 25-bed critical access hospital, PeaceHealth United General Medical Center offers advanced treatment options and short hospital stays. Comprehensive cancer care is provided at PeaceHealth United General's Cancer Center and a variety of surgical procedures is available at the Surgery & Orthopedics Center. Primary and specialty care is provided by PeaceHealth Medical Group._
**Job Summary**
Demonstrates compassion, respect and caring while working within the scope of practice of Physician to provide safe and efficient care to patients and assistance to their families and visitors. Works collaboratively with all other healthcare team members toward the best outcomes for the patient and the organization. Provides professional services to the hospital and its patients.
**Essential Functions**
+ Practice of medicine within the scope of license, training and credentialing.
+ Practice of medicine in accordance with the current standards of care as well as the quality criteria adopted by the clinic.
+ Assess, plan, implement and evaluate individual patient care appropriate to the age of patients served by demonstrating knowledge of the principles of growth and development over the life span.
+ Performs other duties as assigned.
**Qualifications**
**Education**
+ Accredited School of Medicine Required.
+ Required: completion of Internship/Residency Program in area of specialty.
**Experience**
+ Required: Computer experience
**Credentials**
+ Required: Licensed to practice as a physician in the State, and board certified or board eligible and
+ Required : Drug Enforcement Admin Federal Number and
+ Required : Cardiopulmonary Resuscitation
**Skills**
+ Demonstrated expertise in clinical management of patients. (Required)
+ Maintains current knowledge and skills with continuing education. (Required)
+ Must meet all training requirements for specific department. (Required)
+ Able to work varied hours; rigorous on-call and call-back schedule. (Required)
+ Must not be a practitioner excluded from participation in the Medicare or Medicaid program. (Required)
**Department / Location Specific Notes**
**Working Conditions**
Lifting
+ Patient handling no greater than 35 lbs. without the use of assistive equipment and/or devices (NIOSH).
+ Fine motor skills to be able to grasp and control medical equipment and perform precise procedures.
+ Perform hands on CPR at least 20 mins using 100-125 lbs. of force (National Assoc. of EMS Physicians and AHA) Frequency should be seldom or occasionally.
+ Ability to move around area with frequent sitting.
+ Bending/ stooping / reaching occasionally.
+ Lifting (non-patient) up to 20 lbs. occasionally and 5 lbs. frequently.
Environmental Conditions
+ Exposure to biohazard, body fluids and airborne particles.
+ Time spent on site in medical/hospital setting.
Mental/Visual
+ Vision and hearing required within normal limits (glasses, contacts, hearing aids permitted).
+ Ability to communicate and exchange accurate information.
See how PeaceHealth is committed to Inclusivity, Respect for Diversity and Cultural Humility ( .
PeaceHealth has exceptional benefits. ( Affirmative Action Employer/Vets/Disabled in accordance with applicable local, state or federal laws.
REQNUMBER: 77002
PeaceHealth is seeking a Hematology/Oncology physician who could provide per diem coverage based in beautiful Sedro-Woolley, Washington located half-way between Seattle and Vancouver, British Columbia.
Unique opportunity to be part of a larger oncology team in a beautiful, growing community where patients value their physicians and health caregivers. The ideal candidate will be Board Certified.
Why you'll love the practice
+ The cancer center at United General Medical Center (UGMC) has a hub & spoke model with PeaceHealth St. Joseph Cancer Center in Bellingham, WA
+ Full range of services in one location: Medical Oncology and Radiation Oncology, 24/7 emergency contact line, RapidArc radio therapy and SBRT, 9 infusion chairs, resource center with boutique for patients, designated patient navigators
+ Commission on Cancer Accreditation responsibilities
+ Strong primary and specialty care presence in Sedro-Woolley/Burlington area
+ Epic EMR
Position is paid at $282.66/hour and includes medical malpractice coverage with tail coverage. Potential for travel/accommodation stipend and license reimbursement.
**Please reach out to learn more: Manjit Kaur, Physician and Clinician Recruiter;** ** **
Sedro-Woolley, WA, the "Gateway to the North Cascades," is a wonderful blend of incredible scenery, endless outdoor recreation and small-town living! Stroll through historic downtown to see life-size chainsaw art sculptures carved from cedar logs at the annual Loggerodeo. The seasonal Farmers Market offers some of Skagit County's freshest produce, meats, cheeses, flowers, handcrafted goods and snacks, and Riverfront Park offers picnicking and boating beside the Skagit River. There are unlimited opportunities for breathtaking hikes, relaxing camping trips, water activities, bird watching, snow sports, scenic drives and horseback riding. Both Sedro-Woolley and neighboring Burlington, WA (known as "The Hub of Skagit County") offer many Arts, Culture, Entertainment and retail opportunities, including the famous Skagit Tulip Festival. Finally, if you want to visit a bigger city, Sedro-Woolley is a quick 20-minute drive to Bellingham, a 90-minute drive to Seattle, WA and a 90-minute drive to Vancouver, British Columbia.
_A 25-bed critical access hospital, PeaceHealth United General Medical Center offers advanced treatment options and short hospital stays. Comprehensive cancer care is provided at PeaceHealth United General's Cancer Center and a variety of surgical procedures is available at the Surgery & Orthopedics Center. Primary and specialty care is provided by PeaceHealth Medical Group._
**Job Summary**
Demonstrates compassion, respect and caring while working within the scope of practice of Physician to provide safe and efficient care to patients and assistance to their families and visitors. Works collaboratively with all other healthcare team members toward the best outcomes for the patient and the organization. Provides professional services to the hospital and its patients.
**Essential Functions**
+ Practice of medicine within the scope of license, training and credentialing.
+ Practice of medicine in accordance with the current standards of care as well as the quality criteria adopted by the clinic.
+ Assess, plan, implement and evaluate individual patient care appropriate to the age of patients served by demonstrating knowledge of the principles of growth and development over the life span.
+ Performs other duties as assigned.
**Qualifications**
**Education**
+ Accredited School of Medicine Required.
+ Required: completion of Internship/Residency Program in area of specialty.
**Experience**
+ Required: Computer experience
**Credentials**
+ Required: Licensed to practice as a physician in the State, and board certified or board eligible and
+ Required : Drug Enforcement Admin Federal Number and
+ Required : Cardiopulmonary Resuscitation
**Skills**
+ Demonstrated expertise in clinical management of patients. (Required)
+ Maintains current knowledge and skills with continuing education. (Required)
+ Must meet all training requirements for specific department. (Required)
+ Able to work varied hours; rigorous on-call and call-back schedule. (Required)
+ Must not be a practitioner excluded from participation in the Medicare or Medicaid program. (Required)
**Department / Location Specific Notes**
**Working Conditions**
Lifting
+ Patient handling no greater than 35 lbs. without the use of assistive equipment and/or devices (NIOSH).
+ Fine motor skills to be able to grasp and control medical equipment and perform precise procedures.
+ Perform hands on CPR at least 20 mins using 100-125 lbs. of force (National Assoc. of EMS Physicians and AHA) Frequency should be seldom or occasionally.
+ Ability to move around area with frequent sitting.
+ Bending/ stooping / reaching occasionally.
+ Lifting (non-patient) up to 20 lbs. occasionally and 5 lbs. frequently.
Environmental Conditions
+ Exposure to biohazard, body fluids and airborne particles.
+ Time spent on site in medical/hospital setting.
Mental/Visual
+ Vision and hearing required within normal limits (glasses, contacts, hearing aids permitted).
+ Ability to communicate and exchange accurate information.
See how PeaceHealth is committed to Inclusivity, Respect for Diversity and Cultural Humility ( .
PeaceHealth has exceptional benefits. ( Affirmative Action Employer/Vets/Disabled in accordance with applicable local, state or federal laws.
REQNUMBER: 77002
This advertiser has chosen not to accept applicants from your region.
2
Hematology/Oncology Physician - Per Diem
Abbotsford, British Columbia
PeaceHealth
Posted 21 days ago
Job Viewed
Job Description
**Description**
PeaceHealth is seeking a Hematology/Oncology physician who could provide per diem coverage based in beautiful Sedro-Woolley, Washington located half-way between Seattle and Vancouver, British Columbia.
Unique opportunity to be part of a larger oncology team in a beautiful, growing community where patients value their physicians and health caregivers. The ideal candidate will be Board Certified.
Why you'll love the practice
+ The cancer center at United General Medical Center (UGMC) has a hub & spoke model with PeaceHealth St. Joseph Cancer Center in Bellingham, WA
+ Full range of services in one location: Medical Oncology and Radiation Oncology, 24/7 emergency contact line, RapidArc radio therapy and SBRT, 9 infusion chairs, resource center with boutique for patients, designated patient navigators
+ Commission on Cancer Accreditation responsibilities
+ Strong primary and specialty care presence in Sedro-Woolley/Burlington area
+ Epic EMR
Position is paid at $282.66/hour and includes medical malpractice coverage with tail coverage. Potential for travel/accommodation stipend and license reimbursement.
**Please reach out to learn more: Manjit Kaur, Physician and Clinician Recruiter;** ** **
Sedro-Woolley, WA, the "Gateway to the North Cascades," is a wonderful blend of incredible scenery, endless outdoor recreation and small-town living! Stroll through historic downtown to see life-size chainsaw art sculptures carved from cedar logs at the annual Loggerodeo. The seasonal Farmers Market offers some of Skagit County's freshest produce, meats, cheeses, flowers, handcrafted goods and snacks, and Riverfront Park offers picnicking and boating beside the Skagit River. There are unlimited opportunities for breathtaking hikes, relaxing camping trips, water activities, bird watching, snow sports, scenic drives and horseback riding. Both Sedro-Woolley and neighboring Burlington, WA (known as "The Hub of Skagit County") offer many Arts, Culture, Entertainment and retail opportunities, including the famous Skagit Tulip Festival. Finally, if you want to visit a bigger city, Sedro-Woolley is a quick 20-minute drive to Bellingham, a 90-minute drive to Seattle, WA and a 90-minute drive to Vancouver, British Columbia.
_A 25-bed critical access hospital, PeaceHealth United General Medical Center offers advanced treatment options and short hospital stays. Comprehensive cancer care is provided at PeaceHealth United General's Cancer Center and a variety of surgical procedures is available at the Surgery & Orthopedics Center. Primary and specialty care is provided by PeaceHealth Medical Group._
**Job Summary**
Demonstrates compassion, respect and caring while working within the scope of practice of Physician to provide safe and efficient care to patients and assistance to their families and visitors. Works collaboratively with all other healthcare team members toward the best outcomes for the patient and the organization. Provides professional services to the hospital and its patients.
**Essential Functions**
+ Practice of medicine within the scope of license, training and credentialing.
+ Practice of medicine in accordance with the current standards of care as well as the quality criteria adopted by the clinic.
+ Assess, plan, implement and evaluate individual patient care appropriate to the age of patients served by demonstrating knowledge of the principles of growth and development over the life span.
+ Performs other duties as assigned.
**Qualifications**
**Education**
+ Accredited School of Medicine Required.
+ Required: completion of Internship/Residency Program in area of specialty.
**Experience**
+ Required: Computer experience
**Credentials**
+ Required: Licensed to practice as a physician in the State, and board certified or board eligible and
+ Required : Drug Enforcement Admin Federal Number and
+ Required : Cardiopulmonary Resuscitation
**Skills**
+ Demonstrated expertise in clinical management of patients. (Required)
+ Maintains current knowledge and skills with continuing education. (Required)
+ Must meet all training requirements for specific department. (Required)
+ Able to work varied hours; rigorous on-call and call-back schedule. (Required)
+ Must not be a practitioner excluded from participation in the Medicare or Medicaid program. (Required)
**Department / Location Specific Notes**
**Working Conditions**
Lifting
+ Patient handling no greater than 35 lbs. without the use of assistive equipment and/or devices (NIOSH).
+ Fine motor skills to be able to grasp and control medical equipment and perform precise procedures.
+ Perform hands on CPR at least 20 mins using 100-125 lbs. of force (National Assoc. of EMS Physicians and AHA) Frequency should be seldom or occasionally.
+ Ability to move around area with frequent sitting.
+ Bending/ stooping / reaching occasionally.
+ Lifting (non-patient) up to 20 lbs. occasionally and 5 lbs. frequently.
Environmental Conditions
+ Exposure to biohazard, body fluids and airborne particles.
+ Time spent on site in medical/hospital setting.
Mental/Visual
+ Vision and hearing required within normal limits (glasses, contacts, hearing aids permitted).
+ Ability to communicate and exchange accurate information.
See how PeaceHealth is committed to Inclusivity, Respect for Diversity and Cultural Humility ( .
PeaceHealth has exceptional benefits. ( Affirmative Action Employer/Vets/Disabled in accordance with applicable local, state or federal laws.
REQNUMBER: 77002
PeaceHealth is seeking a Hematology/Oncology physician who could provide per diem coverage based in beautiful Sedro-Woolley, Washington located half-way between Seattle and Vancouver, British Columbia.
Unique opportunity to be part of a larger oncology team in a beautiful, growing community where patients value their physicians and health caregivers. The ideal candidate will be Board Certified.
Why you'll love the practice
+ The cancer center at United General Medical Center (UGMC) has a hub & spoke model with PeaceHealth St. Joseph Cancer Center in Bellingham, WA
+ Full range of services in one location: Medical Oncology and Radiation Oncology, 24/7 emergency contact line, RapidArc radio therapy and SBRT, 9 infusion chairs, resource center with boutique for patients, designated patient navigators
+ Commission on Cancer Accreditation responsibilities
+ Strong primary and specialty care presence in Sedro-Woolley/Burlington area
+ Epic EMR
Position is paid at $282.66/hour and includes medical malpractice coverage with tail coverage. Potential for travel/accommodation stipend and license reimbursement.
**Please reach out to learn more: Manjit Kaur, Physician and Clinician Recruiter;** ** **
Sedro-Woolley, WA, the "Gateway to the North Cascades," is a wonderful blend of incredible scenery, endless outdoor recreation and small-town living! Stroll through historic downtown to see life-size chainsaw art sculptures carved from cedar logs at the annual Loggerodeo. The seasonal Farmers Market offers some of Skagit County's freshest produce, meats, cheeses, flowers, handcrafted goods and snacks, and Riverfront Park offers picnicking and boating beside the Skagit River. There are unlimited opportunities for breathtaking hikes, relaxing camping trips, water activities, bird watching, snow sports, scenic drives and horseback riding. Both Sedro-Woolley and neighboring Burlington, WA (known as "The Hub of Skagit County") offer many Arts, Culture, Entertainment and retail opportunities, including the famous Skagit Tulip Festival. Finally, if you want to visit a bigger city, Sedro-Woolley is a quick 20-minute drive to Bellingham, a 90-minute drive to Seattle, WA and a 90-minute drive to Vancouver, British Columbia.
_A 25-bed critical access hospital, PeaceHealth United General Medical Center offers advanced treatment options and short hospital stays. Comprehensive cancer care is provided at PeaceHealth United General's Cancer Center and a variety of surgical procedures is available at the Surgery & Orthopedics Center. Primary and specialty care is provided by PeaceHealth Medical Group._
**Job Summary**
Demonstrates compassion, respect and caring while working within the scope of practice of Physician to provide safe and efficient care to patients and assistance to their families and visitors. Works collaboratively with all other healthcare team members toward the best outcomes for the patient and the organization. Provides professional services to the hospital and its patients.
**Essential Functions**
+ Practice of medicine within the scope of license, training and credentialing.
+ Practice of medicine in accordance with the current standards of care as well as the quality criteria adopted by the clinic.
+ Assess, plan, implement and evaluate individual patient care appropriate to the age of patients served by demonstrating knowledge of the principles of growth and development over the life span.
+ Performs other duties as assigned.
**Qualifications**
**Education**
+ Accredited School of Medicine Required.
+ Required: completion of Internship/Residency Program in area of specialty.
**Experience**
+ Required: Computer experience
**Credentials**
+ Required: Licensed to practice as a physician in the State, and board certified or board eligible and
+ Required : Drug Enforcement Admin Federal Number and
+ Required : Cardiopulmonary Resuscitation
**Skills**
+ Demonstrated expertise in clinical management of patients. (Required)
+ Maintains current knowledge and skills with continuing education. (Required)
+ Must meet all training requirements for specific department. (Required)
+ Able to work varied hours; rigorous on-call and call-back schedule. (Required)
+ Must not be a practitioner excluded from participation in the Medicare or Medicaid program. (Required)
**Department / Location Specific Notes**
**Working Conditions**
Lifting
+ Patient handling no greater than 35 lbs. without the use of assistive equipment and/or devices (NIOSH).
+ Fine motor skills to be able to grasp and control medical equipment and perform precise procedures.
+ Perform hands on CPR at least 20 mins using 100-125 lbs. of force (National Assoc. of EMS Physicians and AHA) Frequency should be seldom or occasionally.
+ Ability to move around area with frequent sitting.
+ Bending/ stooping / reaching occasionally.
+ Lifting (non-patient) up to 20 lbs. occasionally and 5 lbs. frequently.
Environmental Conditions
+ Exposure to biohazard, body fluids and airborne particles.
+ Time spent on site in medical/hospital setting.
Mental/Visual
+ Vision and hearing required within normal limits (glasses, contacts, hearing aids permitted).
+ Ability to communicate and exchange accurate information.
See how PeaceHealth is committed to Inclusivity, Respect for Diversity and Cultural Humility ( .
PeaceHealth has exceptional benefits. ( Affirmative Action Employer/Vets/Disabled in accordance with applicable local, state or federal laws.
REQNUMBER: 77002
This advertiser has chosen not to accept applicants from your region.
3
Hematology/Oncology Physician - Per Diem
Vancouver, British Columbia
PeaceHealth
Posted 21 days ago
Job Viewed
Job Description
**Description**
PeaceHealth is seeking a Hematology/Oncology physician who could provide per diem coverage based in beautiful Sedro-Woolley, Washington located half-way between Seattle and Vancouver, British Columbia.
Unique opportunity to be part of a larger oncology team in a beautiful, growing community where patients value their physicians and health caregivers. The ideal candidate will be Board Certified.
Why you'll love the practice
+ The cancer center at United General Medical Center (UGMC) has a hub & spoke model with PeaceHealth St. Joseph Cancer Center in Bellingham, WA
+ Full range of services in one location: Medical Oncology and Radiation Oncology, 24/7 emergency contact line, RapidArc radio therapy and SBRT, 9 infusion chairs, resource center with boutique for patients, designated patient navigators
+ Commission on Cancer Accreditation responsibilities
+ Strong primary and specialty care presence in Sedro-Woolley/Burlington area
+ Epic EMR
Position is paid at $282.66/hour and includes medical malpractice coverage with tail coverage. Potential for travel/accommodation stipend and license reimbursement.
**Please reach out to learn more: Manjit Kaur, Physician and Clinician Recruiter;** ** **
Sedro-Woolley, WA, the "Gateway to the North Cascades," is a wonderful blend of incredible scenery, endless outdoor recreation and small-town living! Stroll through historic downtown to see life-size chainsaw art sculptures carved from cedar logs at the annual Loggerodeo. The seasonal Farmers Market offers some of Skagit County's freshest produce, meats, cheeses, flowers, handcrafted goods and snacks, and Riverfront Park offers picnicking and boating beside the Skagit River. There are unlimited opportunities for breathtaking hikes, relaxing camping trips, water activities, bird watching, snow sports, scenic drives and horseback riding. Both Sedro-Woolley and neighboring Burlington, WA (known as "The Hub of Skagit County") offer many Arts, Culture, Entertainment and retail opportunities, including the famous Skagit Tulip Festival. Finally, if you want to visit a bigger city, Sedro-Woolley is a quick 20-minute drive to Bellingham, a 90-minute drive to Seattle, WA and a 90-minute drive to Vancouver, British Columbia.
_A 25-bed critical access hospital, PeaceHealth United General Medical Center offers advanced treatment options and short hospital stays. Comprehensive cancer care is provided at PeaceHealth United General's Cancer Center and a variety of surgical procedures is available at the Surgery & Orthopedics Center. Primary and specialty care is provided by PeaceHealth Medical Group._
**Job Summary**
Demonstrates compassion, respect and caring while working within the scope of practice of Physician to provide safe and efficient care to patients and assistance to their families and visitors. Works collaboratively with all other healthcare team members toward the best outcomes for the patient and the organization. Provides professional services to the hospital and its patients.
**Essential Functions**
+ Practice of medicine within the scope of license, training and credentialing.
+ Practice of medicine in accordance with the current standards of care as well as the quality criteria adopted by the clinic.
+ Assess, plan, implement and evaluate individual patient care appropriate to the age of patients served by demonstrating knowledge of the principles of growth and development over the life span.
+ Performs other duties as assigned.
**Qualifications**
**Education**
+ Accredited School of Medicine Required.
+ Required: completion of Internship/Residency Program in area of specialty.
**Experience**
+ Required: Computer experience
**Credentials**
+ Required: Licensed to practice as a physician in the State, and board certified or board eligible and
+ Required : Drug Enforcement Admin Federal Number and
+ Required : Cardiopulmonary Resuscitation
**Skills**
+ Demonstrated expertise in clinical management of patients. (Required)
+ Maintains current knowledge and skills with continuing education. (Required)
+ Must meet all training requirements for specific department. (Required)
+ Able to work varied hours; rigorous on-call and call-back schedule. (Required)
+ Must not be a practitioner excluded from participation in the Medicare or Medicaid program. (Required)
**Department / Location Specific Notes**
**Working Conditions**
Lifting
+ Patient handling no greater than 35 lbs. without the use of assistive equipment and/or devices (NIOSH).
+ Fine motor skills to be able to grasp and control medical equipment and perform precise procedures.
+ Perform hands on CPR at least 20 mins using 100-125 lbs. of force (National Assoc. of EMS Physicians and AHA) Frequency should be seldom or occasionally.
+ Ability to move around area with frequent sitting.
+ Bending/ stooping / reaching occasionally.
+ Lifting (non-patient) up to 20 lbs. occasionally and 5 lbs. frequently.
Environmental Conditions
+ Exposure to biohazard, body fluids and airborne particles.
+ Time spent on site in medical/hospital setting.
Mental/Visual
+ Vision and hearing required within normal limits (glasses, contacts, hearing aids permitted).
+ Ability to communicate and exchange accurate information.
See how PeaceHealth is committed to Inclusivity, Respect for Diversity and Cultural Humility ( .
PeaceHealth has exceptional benefits. ( Affirmative Action Employer/Vets/Disabled in accordance with applicable local, state or federal laws.
REQNUMBER: 77002
PeaceHealth is seeking a Hematology/Oncology physician who could provide per diem coverage based in beautiful Sedro-Woolley, Washington located half-way between Seattle and Vancouver, British Columbia.
Unique opportunity to be part of a larger oncology team in a beautiful, growing community where patients value their physicians and health caregivers. The ideal candidate will be Board Certified.
Why you'll love the practice
+ The cancer center at United General Medical Center (UGMC) has a hub & spoke model with PeaceHealth St. Joseph Cancer Center in Bellingham, WA
+ Full range of services in one location: Medical Oncology and Radiation Oncology, 24/7 emergency contact line, RapidArc radio therapy and SBRT, 9 infusion chairs, resource center with boutique for patients, designated patient navigators
+ Commission on Cancer Accreditation responsibilities
+ Strong primary and specialty care presence in Sedro-Woolley/Burlington area
+ Epic EMR
Position is paid at $282.66/hour and includes medical malpractice coverage with tail coverage. Potential for travel/accommodation stipend and license reimbursement.
**Please reach out to learn more: Manjit Kaur, Physician and Clinician Recruiter;** ** **
Sedro-Woolley, WA, the "Gateway to the North Cascades," is a wonderful blend of incredible scenery, endless outdoor recreation and small-town living! Stroll through historic downtown to see life-size chainsaw art sculptures carved from cedar logs at the annual Loggerodeo. The seasonal Farmers Market offers some of Skagit County's freshest produce, meats, cheeses, flowers, handcrafted goods and snacks, and Riverfront Park offers picnicking and boating beside the Skagit River. There are unlimited opportunities for breathtaking hikes, relaxing camping trips, water activities, bird watching, snow sports, scenic drives and horseback riding. Both Sedro-Woolley and neighboring Burlington, WA (known as "The Hub of Skagit County") offer many Arts, Culture, Entertainment and retail opportunities, including the famous Skagit Tulip Festival. Finally, if you want to visit a bigger city, Sedro-Woolley is a quick 20-minute drive to Bellingham, a 90-minute drive to Seattle, WA and a 90-minute drive to Vancouver, British Columbia.
_A 25-bed critical access hospital, PeaceHealth United General Medical Center offers advanced treatment options and short hospital stays. Comprehensive cancer care is provided at PeaceHealth United General's Cancer Center and a variety of surgical procedures is available at the Surgery & Orthopedics Center. Primary and specialty care is provided by PeaceHealth Medical Group._
**Job Summary**
Demonstrates compassion, respect and caring while working within the scope of practice of Physician to provide safe and efficient care to patients and assistance to their families and visitors. Works collaboratively with all other healthcare team members toward the best outcomes for the patient and the organization. Provides professional services to the hospital and its patients.
**Essential Functions**
+ Practice of medicine within the scope of license, training and credentialing.
+ Practice of medicine in accordance with the current standards of care as well as the quality criteria adopted by the clinic.
+ Assess, plan, implement and evaluate individual patient care appropriate to the age of patients served by demonstrating knowledge of the principles of growth and development over the life span.
+ Performs other duties as assigned.
**Qualifications**
**Education**
+ Accredited School of Medicine Required.
+ Required: completion of Internship/Residency Program in area of specialty.
**Experience**
+ Required: Computer experience
**Credentials**
+ Required: Licensed to practice as a physician in the State, and board certified or board eligible and
+ Required : Drug Enforcement Admin Federal Number and
+ Required : Cardiopulmonary Resuscitation
**Skills**
+ Demonstrated expertise in clinical management of patients. (Required)
+ Maintains current knowledge and skills with continuing education. (Required)
+ Must meet all training requirements for specific department. (Required)
+ Able to work varied hours; rigorous on-call and call-back schedule. (Required)
+ Must not be a practitioner excluded from participation in the Medicare or Medicaid program. (Required)
**Department / Location Specific Notes**
**Working Conditions**
Lifting
+ Patient handling no greater than 35 lbs. without the use of assistive equipment and/or devices (NIOSH).
+ Fine motor skills to be able to grasp and control medical equipment and perform precise procedures.
+ Perform hands on CPR at least 20 mins using 100-125 lbs. of force (National Assoc. of EMS Physicians and AHA) Frequency should be seldom or occasionally.
+ Ability to move around area with frequent sitting.
+ Bending/ stooping / reaching occasionally.
+ Lifting (non-patient) up to 20 lbs. occasionally and 5 lbs. frequently.
Environmental Conditions
+ Exposure to biohazard, body fluids and airborne particles.
+ Time spent on site in medical/hospital setting.
Mental/Visual
+ Vision and hearing required within normal limits (glasses, contacts, hearing aids permitted).
+ Ability to communicate and exchange accurate information.
See how PeaceHealth is committed to Inclusivity, Respect for Diversity and Cultural Humility ( .
PeaceHealth has exceptional benefits. ( Affirmative Action Employer/Vets/Disabled in accordance with applicable local, state or federal laws.
REQNUMBER: 77002
This advertiser has chosen not to accept applicants from your region.
4
Hematology/Oncology Physician - Per Diem
Victoria, British Columbia
PeaceHealth
Posted 21 days ago
Job Viewed
Job Description
**Description**
PeaceHealth is seeking a Hematology/Oncology physician who could provide per diem coverage based in beautiful Sedro-Woolley, Washington located half-way between Seattle and Vancouver, British Columbia.
Unique opportunity to be part of a larger oncology team in a beautiful, growing community where patients value their physicians and health caregivers. The ideal candidate will be Board Certified.
Why you'll love the practice
+ The cancer center at United General Medical Center (UGMC) has a hub & spoke model with PeaceHealth St. Joseph Cancer Center in Bellingham, WA
+ Full range of services in one location: Medical Oncology and Radiation Oncology, 24/7 emergency contact line, RapidArc radio therapy and SBRT, 9 infusion chairs, resource center with boutique for patients, designated patient navigators
+ Commission on Cancer Accreditation responsibilities
+ Strong primary and specialty care presence in Sedro-Woolley/Burlington area
+ Epic EMR
Position is paid at $282.66/hour and includes medical malpractice coverage with tail coverage. Potential for travel/accommodation stipend and license reimbursement.
**Please reach out to learn more: Manjit Kaur, Physician and Clinician Recruiter;** ** **
Sedro-Woolley, WA, the "Gateway to the North Cascades," is a wonderful blend of incredible scenery, endless outdoor recreation and small-town living! Stroll through historic downtown to see life-size chainsaw art sculptures carved from cedar logs at the annual Loggerodeo. The seasonal Farmers Market offers some of Skagit County's freshest produce, meats, cheeses, flowers, handcrafted goods and snacks, and Riverfront Park offers picnicking and boating beside the Skagit River. There are unlimited opportunities for breathtaking hikes, relaxing camping trips, water activities, bird watching, snow sports, scenic drives and horseback riding. Both Sedro-Woolley and neighboring Burlington, WA (known as "The Hub of Skagit County") offer many Arts, Culture, Entertainment and retail opportunities, including the famous Skagit Tulip Festival. Finally, if you want to visit a bigger city, Sedro-Woolley is a quick 20-minute drive to Bellingham, a 90-minute drive to Seattle, WA and a 90-minute drive to Vancouver, British Columbia.
_A 25-bed critical access hospital, PeaceHealth United General Medical Center offers advanced treatment options and short hospital stays. Comprehensive cancer care is provided at PeaceHealth United General's Cancer Center and a variety of surgical procedures is available at the Surgery & Orthopedics Center. Primary and specialty care is provided by PeaceHealth Medical Group._
**Job Summary**
Demonstrates compassion, respect and caring while working within the scope of practice of Physician to provide safe and efficient care to patients and assistance to their families and visitors. Works collaboratively with all other healthcare team members toward the best outcomes for the patient and the organization. Provides professional services to the hospital and its patients.
**Essential Functions**
+ Practice of medicine within the scope of license, training and credentialing.
+ Practice of medicine in accordance with the current standards of care as well as the quality criteria adopted by the clinic.
+ Assess, plan, implement and evaluate individual patient care appropriate to the age of patients served by demonstrating knowledge of the principles of growth and development over the life span.
+ Performs other duties as assigned.
**Qualifications**
**Education**
+ Accredited School of Medicine Required.
+ Required: completion of Internship/Residency Program in area of specialty.
**Experience**
+ Required: Computer experience
**Credentials**
+ Required: Licensed to practice as a physician in the State, and board certified or board eligible and
+ Required : Drug Enforcement Admin Federal Number and
+ Required : Cardiopulmonary Resuscitation
**Skills**
+ Demonstrated expertise in clinical management of patients. (Required)
+ Maintains current knowledge and skills with continuing education. (Required)
+ Must meet all training requirements for specific department. (Required)
+ Able to work varied hours; rigorous on-call and call-back schedule. (Required)
+ Must not be a practitioner excluded from participation in the Medicare or Medicaid program. (Required)
**Department / Location Specific Notes**
**Working Conditions**
Lifting
+ Patient handling no greater than 35 lbs. without the use of assistive equipment and/or devices (NIOSH).
+ Fine motor skills to be able to grasp and control medical equipment and perform precise procedures.
+ Perform hands on CPR at least 20 mins using 100-125 lbs. of force (National Assoc. of EMS Physicians and AHA) Frequency should be seldom or occasionally.
+ Ability to move around area with frequent sitting.
+ Bending/ stooping / reaching occasionally.
+ Lifting (non-patient) up to 20 lbs. occasionally and 5 lbs. frequently.
Environmental Conditions
+ Exposure to biohazard, body fluids and airborne particles.
+ Time spent on site in medical/hospital setting.
Mental/Visual
+ Vision and hearing required within normal limits (glasses, contacts, hearing aids permitted).
+ Ability to communicate and exchange accurate information.
See how PeaceHealth is committed to Inclusivity, Respect for Diversity and Cultural Humility ( .
PeaceHealth has exceptional benefits. ( Affirmative Action Employer/Vets/Disabled in accordance with applicable local, state or federal laws.
REQNUMBER: 77002
PeaceHealth is seeking a Hematology/Oncology physician who could provide per diem coverage based in beautiful Sedro-Woolley, Washington located half-way between Seattle and Vancouver, British Columbia.
Unique opportunity to be part of a larger oncology team in a beautiful, growing community where patients value their physicians and health caregivers. The ideal candidate will be Board Certified.
Why you'll love the practice
+ The cancer center at United General Medical Center (UGMC) has a hub & spoke model with PeaceHealth St. Joseph Cancer Center in Bellingham, WA
+ Full range of services in one location: Medical Oncology and Radiation Oncology, 24/7 emergency contact line, RapidArc radio therapy and SBRT, 9 infusion chairs, resource center with boutique for patients, designated patient navigators
+ Commission on Cancer Accreditation responsibilities
+ Strong primary and specialty care presence in Sedro-Woolley/Burlington area
+ Epic EMR
Position is paid at $282.66/hour and includes medical malpractice coverage with tail coverage. Potential for travel/accommodation stipend and license reimbursement.
**Please reach out to learn more: Manjit Kaur, Physician and Clinician Recruiter;** ** **
Sedro-Woolley, WA, the "Gateway to the North Cascades," is a wonderful blend of incredible scenery, endless outdoor recreation and small-town living! Stroll through historic downtown to see life-size chainsaw art sculptures carved from cedar logs at the annual Loggerodeo. The seasonal Farmers Market offers some of Skagit County's freshest produce, meats, cheeses, flowers, handcrafted goods and snacks, and Riverfront Park offers picnicking and boating beside the Skagit River. There are unlimited opportunities for breathtaking hikes, relaxing camping trips, water activities, bird watching, snow sports, scenic drives and horseback riding. Both Sedro-Woolley and neighboring Burlington, WA (known as "The Hub of Skagit County") offer many Arts, Culture, Entertainment and retail opportunities, including the famous Skagit Tulip Festival. Finally, if you want to visit a bigger city, Sedro-Woolley is a quick 20-minute drive to Bellingham, a 90-minute drive to Seattle, WA and a 90-minute drive to Vancouver, British Columbia.
_A 25-bed critical access hospital, PeaceHealth United General Medical Center offers advanced treatment options and short hospital stays. Comprehensive cancer care is provided at PeaceHealth United General's Cancer Center and a variety of surgical procedures is available at the Surgery & Orthopedics Center. Primary and specialty care is provided by PeaceHealth Medical Group._
**Job Summary**
Demonstrates compassion, respect and caring while working within the scope of practice of Physician to provide safe and efficient care to patients and assistance to their families and visitors. Works collaboratively with all other healthcare team members toward the best outcomes for the patient and the organization. Provides professional services to the hospital and its patients.
**Essential Functions**
+ Practice of medicine within the scope of license, training and credentialing.
+ Practice of medicine in accordance with the current standards of care as well as the quality criteria adopted by the clinic.
+ Assess, plan, implement and evaluate individual patient care appropriate to the age of patients served by demonstrating knowledge of the principles of growth and development over the life span.
+ Performs other duties as assigned.
**Qualifications**
**Education**
+ Accredited School of Medicine Required.
+ Required: completion of Internship/Residency Program in area of specialty.
**Experience**
+ Required: Computer experience
**Credentials**
+ Required: Licensed to practice as a physician in the State, and board certified or board eligible and
+ Required : Drug Enforcement Admin Federal Number and
+ Required : Cardiopulmonary Resuscitation
**Skills**
+ Demonstrated expertise in clinical management of patients. (Required)
+ Maintains current knowledge and skills with continuing education. (Required)
+ Must meet all training requirements for specific department. (Required)
+ Able to work varied hours; rigorous on-call and call-back schedule. (Required)
+ Must not be a practitioner excluded from participation in the Medicare or Medicaid program. (Required)
**Department / Location Specific Notes**
**Working Conditions**
Lifting
+ Patient handling no greater than 35 lbs. without the use of assistive equipment and/or devices (NIOSH).
+ Fine motor skills to be able to grasp and control medical equipment and perform precise procedures.
+ Perform hands on CPR at least 20 mins using 100-125 lbs. of force (National Assoc. of EMS Physicians and AHA) Frequency should be seldom or occasionally.
+ Ability to move around area with frequent sitting.
+ Bending/ stooping / reaching occasionally.
+ Lifting (non-patient) up to 20 lbs. occasionally and 5 lbs. frequently.
Environmental Conditions
+ Exposure to biohazard, body fluids and airborne particles.
+ Time spent on site in medical/hospital setting.
Mental/Visual
+ Vision and hearing required within normal limits (glasses, contacts, hearing aids permitted).
+ Ability to communicate and exchange accurate information.
See how PeaceHealth is committed to Inclusivity, Respect for Diversity and Cultural Humility ( .
PeaceHealth has exceptional benefits. ( Affirmative Action Employer/Vets/Disabled in accordance with applicable local, state or federal laws.
REQNUMBER: 77002
This advertiser has chosen not to accept applicants from your region.
5
Medical Director - Hematology/Oncology - Remote U.S/Canada
Toronto, Ontario
ThermoFisher Scientific
Posted today
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
As part of the Thermo Fisher Scientific team, youu2019ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worldu2019s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
**Summarized Purpose:**
Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides medical consultation to clients, investigators and project team members and supports business development activities. Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports (e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g. labelling reconciliation documents, CTD modules, REMS, RMP and CSR).
**General Support:**
Ensures tasks delegated to pharmacovigilance are properly executed. Adheres to applicable regulations and ICH guidelines regarding clinical trials, regulatory documents, and safety issues. Adheres to client SOPs/directives and project specific WPDs for assigned projects. Adheres to PPDu2019s corporate policies and SOPs/WPDs. Provides medical consultation to team members and answer all study related medical questions. Communicates clearly with associates and clients, maintaining an open line of communication to ensure all procedures are followed appropriately. Provides therapeutic training and protocol training on assigned studies, as requested. Performs data review as specified in the client contract and data validation manual including review of coding listings and/or full safety data to assess for potential safety concerns. Assists in writing (interpretation of safety and efficacy data) and/or review of CSR, IND/NDA report, ICSR, signal detection reports, periodic reports, RMP, REMS, CTD modules, etc. to ensure that the medical content is accurate and complete. Contributes to departmental process improvement initiatives.
**Clinical Trial Support:**
Monitors all safety variables (AE, laboratory abnormalities, changes in patient medical status, evaluation of prescribed concomitant medication for protocol restrictions, and un-blinding requests) of clinical studies. Discusses all medical concerns with principal investigators and clients (e.g. discussion regarding interpretation of inclusion/exclusion criteria) raised during the course of a study, using proper medical judgment in the interpretation and decision making with regard to clinical situations as they relate to the investigational study. Provides medical review of adverse events of special interest, serious adverse events and clinical outcomes events reported by study sites
**Marketed Products Support:**
Manages signal detection activities, scientifically reviews aggregate reports, contributes to label updates, supports dossier maintenance and risk management activities. Medically reviews adverse event and serious adverse event data from all sources (solicited, spontaneous, literature, etc) as contracted.
**Education and Experience:**
MD required with specialization/formal training in Oncology or Hemato-Oncology (active medical license and board certifications are preferred, but not required).
Clinical experience in treating patients associated with the applicants training (comparable to 2 years)
**and one**
of the following:
Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; Or
Direct experience in safety/Pharmacovigilance medical monitoring (comparable to 2 years).
_In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role._
**Knowledge, Skills and Abilities:**
Therapeutic expertise across one or more medical specialty or sub-specialties (one being Oncology or Hemato-Oncology)
Excellent interpersonal skills, influencing and team building skills
Understanding of guidelines (FDA, ICH, EMA and GCP)
Working knowledge of biostatistics, data management, and clinical operations procedures
Ability to act as a mentor/trainer to other staff within pharmacovigilance
Strong, well supported decision-making, problem solving, organizational skills and analytical skills
Excellent oral and written communication skills
Working knowledge of relevant safety databases (e.g. MedDRA)
Flexibility to travel domestically and internationally for short periods
Ability to work independently, analyse work with attention to detail, process and prioritize sensitive complex information
Proficiency in computer productivity applications (e.g. word processor, spreadsheets and presentations) required
Fluent in spoken and written English
Capable of multitasking and good organization skills
**Working Conditions and Environment:**
Work is performed in an office environment with exposure to electrical office equipment.
Occasional drives to site locations with occasional travel both domestic and international.
**Physical Requirements:**
Frequently stationary for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Frequent mobility required.
Occasional crouching, stooping, bending and twisting of upper body and neck.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
Frequently interacts with others to obtain or relate information to diverse groups.
Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
Regular and consistent attendance.
**Benefits:**
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
As part of the Thermo Fisher Scientific team, youu2019ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worldu2019s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
**Summarized Purpose:**
Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides medical consultation to clients, investigators and project team members and supports business development activities. Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports (e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g. labelling reconciliation documents, CTD modules, REMS, RMP and CSR).
**General Support:**
Ensures tasks delegated to pharmacovigilance are properly executed. Adheres to applicable regulations and ICH guidelines regarding clinical trials, regulatory documents, and safety issues. Adheres to client SOPs/directives and project specific WPDs for assigned projects. Adheres to PPDu2019s corporate policies and SOPs/WPDs. Provides medical consultation to team members and answer all study related medical questions. Communicates clearly with associates and clients, maintaining an open line of communication to ensure all procedures are followed appropriately. Provides therapeutic training and protocol training on assigned studies, as requested. Performs data review as specified in the client contract and data validation manual including review of coding listings and/or full safety data to assess for potential safety concerns. Assists in writing (interpretation of safety and efficacy data) and/or review of CSR, IND/NDA report, ICSR, signal detection reports, periodic reports, RMP, REMS, CTD modules, etc. to ensure that the medical content is accurate and complete. Contributes to departmental process improvement initiatives.
**Clinical Trial Support:**
Monitors all safety variables (AE, laboratory abnormalities, changes in patient medical status, evaluation of prescribed concomitant medication for protocol restrictions, and un-blinding requests) of clinical studies. Discusses all medical concerns with principal investigators and clients (e.g. discussion regarding interpretation of inclusion/exclusion criteria) raised during the course of a study, using proper medical judgment in the interpretation and decision making with regard to clinical situations as they relate to the investigational study. Provides medical review of adverse events of special interest, serious adverse events and clinical outcomes events reported by study sites
**Marketed Products Support:**
Manages signal detection activities, scientifically reviews aggregate reports, contributes to label updates, supports dossier maintenance and risk management activities. Medically reviews adverse event and serious adverse event data from all sources (solicited, spontaneous, literature, etc) as contracted.
**Education and Experience:**
MD required with specialization/formal training in Oncology or Hemato-Oncology (active medical license and board certifications are preferred, but not required).
Clinical experience in treating patients associated with the applicants training (comparable to 2 years)
**and one**
of the following:
Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; Or
Direct experience in safety/Pharmacovigilance medical monitoring (comparable to 2 years).
_In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role._
**Knowledge, Skills and Abilities:**
Therapeutic expertise across one or more medical specialty or sub-specialties (one being Oncology or Hemato-Oncology)
Excellent interpersonal skills, influencing and team building skills
Understanding of guidelines (FDA, ICH, EMA and GCP)
Working knowledge of biostatistics, data management, and clinical operations procedures
Ability to act as a mentor/trainer to other staff within pharmacovigilance
Strong, well supported decision-making, problem solving, organizational skills and analytical skills
Excellent oral and written communication skills
Working knowledge of relevant safety databases (e.g. MedDRA)
Flexibility to travel domestically and internationally for short periods
Ability to work independently, analyse work with attention to detail, process and prioritize sensitive complex information
Proficiency in computer productivity applications (e.g. word processor, spreadsheets and presentations) required
Fluent in spoken and written English
Capable of multitasking and good organization skills
**Working Conditions and Environment:**
Work is performed in an office environment with exposure to electrical office equipment.
Occasional drives to site locations with occasional travel both domestic and international.
**Physical Requirements:**
Frequently stationary for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Frequent mobility required.
Occasional crouching, stooping, bending and twisting of upper body and neck.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
Frequently interacts with others to obtain or relate information to diverse groups.
Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
Regular and consistent attendance.
**Benefits:**
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.
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Medical Director - Hematology/Oncology - Remote U.S/Canada
Toronto, Ontario
ThermoFisher Scientific
Posted today
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
As part of the Thermo Fisher Scientific team, youu2019ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worldu2019s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
**Summarized Purpose:**
Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides medical consultation to clients, investigators and project team members and supports business development activities. Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports (e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g. labelling reconciliation documents, CTD modules, REMS, RMP and CSR).
**General Support:**
Ensures tasks delegated to pharmacovigilance are properly executed. Adheres to applicable regulations and ICH guidelines regarding clinical trials, regulatory documents, and safety issues. Adheres to client SOPs/directives and project specific WPDs for assigned projects. Adheres to PPDu2019s corporate policies and SOPs/WPDs. Provides medical consultation to team members and answer all study related medical questions. Communicates clearly with associates and clients, maintaining an open line of communication to ensure all procedures are followed appropriately. Provides therapeutic training and protocol training on assigned studies, as requested. Performs data review as specified in the client contract and data validation manual including review of coding listings and/or full safety data to assess for potential safety concerns. Assists in writing (interpretation of safety and efficacy data) and/or review of CSR, IND/NDA report, ICSR, signal detection reports, periodic reports, RMP, REMS, CTD modules, etc. to ensure that the medical content is accurate and complete. Contributes to departmental process improvement initiatives.
**Clinical Trial Support:**
Monitors all safety variables (AE, laboratory abnormalities, changes in patient medical status, evaluation of prescribed concomitant medication for protocol restrictions, and un-blinding requests) of clinical studies. Discusses all medical concerns with principal investigators and clients (e.g. discussion regarding interpretation of inclusion/exclusion criteria) raised during the course of a study, using proper medical judgment in the interpretation and decision making with regard to clinical situations as they relate to the investigational study. Provides medical review of adverse events of special interest, serious adverse events and clinical outcomes events reported by study sites
**Marketed Products Support:**
Manages signal detection activities, scientifically reviews aggregate reports, contributes to label updates, supports dossier maintenance and risk management activities. Medically reviews adverse event and serious adverse event data from all sources (solicited, spontaneous, literature, etc) as contracted.
**Education and Experience:**
MD required with specialization/formal training in Oncology or Hemato-Oncology (active medical license and board certifications are preferred, but not required).
Clinical experience in treating patients associated with the applicants training (comparable to 2 years)
**and one**
of the following:
Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; Or
Direct experience in safety/Pharmacovigilance medical monitoring (comparable to 2 years).
_In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role._
**Knowledge, Skills and Abilities:**
Therapeutic expertise across one or more medical specialty or sub-specialties (one being Oncology or Hemato-Oncology)
Excellent interpersonal skills, influencing and team building skills
Understanding of guidelines (FDA, ICH, EMA and GCP)
Working knowledge of biostatistics, data management, and clinical operations procedures
Ability to act as a mentor/trainer to other staff within pharmacovigilance
Strong, well supported decision-making, problem solving, organizational skills and analytical skills
Excellent oral and written communication skills
Working knowledge of relevant safety databases (e.g. MedDRA)
Flexibility to travel domestically and internationally for short periods
Ability to work independently, analyse work with attention to detail, process and prioritize sensitive complex information
Proficiency in computer productivity applications (e.g. word processor, spreadsheets and presentations) required
Fluent in spoken and written English
Capable of multitasking and good organization skills
**Working Conditions and Environment:**
Work is performed in an office environment with exposure to electrical office equipment.
Occasional drives to site locations with occasional travel both domestic and international.
**Physical Requirements:**
Frequently stationary for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Frequent mobility required.
Occasional crouching, stooping, bending and twisting of upper body and neck.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
Frequently interacts with others to obtain or relate information to diverse groups.
Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
Regular and consistent attendance.
**Benefits:**
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
As part of the Thermo Fisher Scientific team, youu2019ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worldu2019s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
**Summarized Purpose:**
Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides medical consultation to clients, investigators and project team members and supports business development activities. Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports (e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g. labelling reconciliation documents, CTD modules, REMS, RMP and CSR).
**General Support:**
Ensures tasks delegated to pharmacovigilance are properly executed. Adheres to applicable regulations and ICH guidelines regarding clinical trials, regulatory documents, and safety issues. Adheres to client SOPs/directives and project specific WPDs for assigned projects. Adheres to PPDu2019s corporate policies and SOPs/WPDs. Provides medical consultation to team members and answer all study related medical questions. Communicates clearly with associates and clients, maintaining an open line of communication to ensure all procedures are followed appropriately. Provides therapeutic training and protocol training on assigned studies, as requested. Performs data review as specified in the client contract and data validation manual including review of coding listings and/or full safety data to assess for potential safety concerns. Assists in writing (interpretation of safety and efficacy data) and/or review of CSR, IND/NDA report, ICSR, signal detection reports, periodic reports, RMP, REMS, CTD modules, etc. to ensure that the medical content is accurate and complete. Contributes to departmental process improvement initiatives.
**Clinical Trial Support:**
Monitors all safety variables (AE, laboratory abnormalities, changes in patient medical status, evaluation of prescribed concomitant medication for protocol restrictions, and un-blinding requests) of clinical studies. Discusses all medical concerns with principal investigators and clients (e.g. discussion regarding interpretation of inclusion/exclusion criteria) raised during the course of a study, using proper medical judgment in the interpretation and decision making with regard to clinical situations as they relate to the investigational study. Provides medical review of adverse events of special interest, serious adverse events and clinical outcomes events reported by study sites
**Marketed Products Support:**
Manages signal detection activities, scientifically reviews aggregate reports, contributes to label updates, supports dossier maintenance and risk management activities. Medically reviews adverse event and serious adverse event data from all sources (solicited, spontaneous, literature, etc) as contracted.
**Education and Experience:**
MD required with specialization/formal training in Oncology or Hemato-Oncology (active medical license and board certifications are preferred, but not required).
Clinical experience in treating patients associated with the applicants training (comparable to 2 years)
**and one**
of the following:
Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; Or
Direct experience in safety/Pharmacovigilance medical monitoring (comparable to 2 years).
_In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role._
**Knowledge, Skills and Abilities:**
Therapeutic expertise across one or more medical specialty or sub-specialties (one being Oncology or Hemato-Oncology)
Excellent interpersonal skills, influencing and team building skills
Understanding of guidelines (FDA, ICH, EMA and GCP)
Working knowledge of biostatistics, data management, and clinical operations procedures
Ability to act as a mentor/trainer to other staff within pharmacovigilance
Strong, well supported decision-making, problem solving, organizational skills and analytical skills
Excellent oral and written communication skills
Working knowledge of relevant safety databases (e.g. MedDRA)
Flexibility to travel domestically and internationally for short periods
Ability to work independently, analyse work with attention to detail, process and prioritize sensitive complex information
Proficiency in computer productivity applications (e.g. word processor, spreadsheets and presentations) required
Fluent in spoken and written English
Capable of multitasking and good organization skills
**Working Conditions and Environment:**
Work is performed in an office environment with exposure to electrical office equipment.
Occasional drives to site locations with occasional travel both domestic and international.
**Physical Requirements:**
Frequently stationary for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Frequent mobility required.
Occasional crouching, stooping, bending and twisting of upper body and neck.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
Frequently interacts with others to obtain or relate information to diverse groups.
Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
Regular and consistent attendance.
**Benefits:**
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.
7