What Rn Clinic Jobs are in Canada?

Registered Practical Nurse (RPN) – Casual Procedural Clinic | Windsor, ON

HealthOPM is currently seeking an experienced Registered Practical Nurse (RPN) to join our casual staffing roster for an outpatient procedural clinic in Windsor, Ontario .

This is an excellent opportunity for RPNs with experience in interventional or procedural settings who are looking for flexible, as-needed work.

Position Details

• Position: Registered Practical Nurse (RPN)
• Location: Windsor, ON
• Employment Type: Casual / On-Call
• Pay Rate: $32.00–$35.00/hour (based on experience)
• Shift Notice: Approximately 1–2 days' notice as clinic coverage is required
• Training: Candidates must be available to attend training before shift starts 

Key Responsibilities

• Room patients, obtain vital signs, and complete pain-related assessments
• Perform focused patient assessments and review medical history
• Initiate IV access and prepare patients for procedures
• Initiate and maintain IV access
• Assist physicians during image-guided and interventional procedures
• Support sterile setup and patient positioning
• Monitor patient vital signs throughout procedures
• Provide post-procedure monitoring, discharge instructions, and patient education
• Maintain accurate EMR documentation
• Follow all clinical, safety, infection prevention, and radiation safety protocols where applicable

Qualifications

• Registered Practical Nurse (RPN) in good standing with the College of Nurses of Ontario (CNO)
• Current Basic Life Support (BLS) certification
• Experience in a procedural or interventional clinical setting
• Strong IV insertion and patient monitoring skills
• Experience with procedural sedation monitoring is an asset
• Comfortable working in a fast-paced outpatient procedural environment

Preferred Experience

Experience in one or more of the following settings:

• Fluoroscopy
• Interventional Pain Clinic
• Endoscopy
• Interventional Radiology
• Cardiac Catheterization Lab
• Operating Room (OR)

Apply Today

If you're an experienced RPN looking for flexible casual work in a procedural clinic environment, we'd love to hear from you.

About the job

Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark , General Catalyst , Peter Thiel , Adam D'Angelo , Larry Summers , and Jack Dorsey .

Position: Registered Nurses
Type: Contract
Compensation: $60–$100/hour
Location: Remote

Role Responsibilities

• Design questions related to the Registered Nurse occupation using your professional experience.
• Collaborate with one of the world’s top AI companies to enhance project outcomes.
• Ensure high-quality content by leveraging domain expertise in nursing .
• Work independently and asynchronously to meet project deadlines.
• Utilize a desktop or laptop computer for project tasks.

Qualifications

Must-Have

• 4+ years full-time work experience as a Registered Nurse.
• Be based in the US, UK, or Canada .

Compensation & Legal

• Hourly contractor with competitive rates based on background and location.

Application Process (Takes 20–30 mins to complete)

• Upload resume
• AI interview based on your resume
• Submit form

Resources & Support

• For details about the interview process and platform information, please check:
• For any help or support, reach out to:

PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Clinical Associate - Hybrid Role - French Speaking - Toronto, Canada
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.
As a Clinical Associate at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
**What You Will Do:**
You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
+ Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.
+ Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation.
+ Collaborate with cross-functional teams including Clinical Operations, Data Management, and Biometrics to support the successful execution of clinical trials.
+ Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures.
+ Support study close-out activities including data cleaning, analysis, and preparation of clinical study reports.
**Your Profile:**
You will bring relevant clinical coordination experience, along with the following qualifications and skills.
Required qualifications and experience:
+ Bachelor's degree in a relevant scientific discipline or healthcare-related field
+ Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry.
+ Strong organizational and time management skills, with the ability to prioritize tasks and manage competing priorities effectively.
+ Excellent attention to detail and problem-solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance.
+ Effective communication and interpersonal skills, with the ability to collaborate cross-functionally and build strong relationships with study teams and clinical sites.
+ Willingness to travel as required (approximately 60%)
**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

Clinical Trial Associate
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.
As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
**What You Will Do:**
Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders.
Key responsibilities include:
+ Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
+ Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
+ Support the preparation of study-related materials, such as informed consent forms and case report forms.
+ Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
+ Contribute to the tracking and reporting of clinical trial metrics and milestones.
**Your Profile:**
You will bring relevant clinical research experience, along with the following qualifications and skills.
Required qualifications and experience:
+ Bachelor's degree in a scientific or healthcare-related field.
+ Prior experience or strong interest in clinical research.
+ Knowledge of clinical trial processes, regulations, and guidelines.
+ Excellent organizational and communication skills.
+ Ability to work collaboratively in a fast-paced environment with attention to detail.
+ Willingness to travel as required (approximately 10%)
_Pay Range ($50,648 - $63,310 CAD) - Actual salary will be based on experience_
**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

Clinical Trial Associate
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.
As a Senior Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks.
**What You Will Do:**
You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges.
Key responsibilities include:
+ Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records.
+ Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements.
+ Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study.
+ Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials.
+ Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success.
**Your Profile:**
You will have a strong foundation in clinical trial management, with the experience to work independently and guide others.
Required qualifications and experience:
+ Bachelor's degree in a relevant scientific discipline or healthcare-related field
+ Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements.
+ Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively.
+ Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management.
+ Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders.
+ Willingness to travel as required (approximately 10%)
**En tant qu'Associé(e) Principal(e) aux Essais Cliniques (Senior Clinical Trial Associate) chez ICON Plc**
En tant que **Senior Clinical Trial Associate (CTA Senior)** chez ICON Plc, vous jouerez un rôle clé dans le soutien à la gestion et à l'exécution des essais cliniques en assurant diverses activités administratives et opérationnelles essentielles au bon déroulement des études.
**Vos responsabilités**
Vous assumerez la responsabilité de plusieurs livrables liés à la gestion des essais cliniques, en mettant à profit votre expertise pour relever des défis complexes et contribuer au succès des projets.
**Principales responsabilités :**
+ Fournir un soutien administratif aux essais cliniques, notamment en gérant la documentation, en coordonnant les réunions et en maintenant à jour les dossiers liés aux études.
+ Participer à la préparation et à la soumission des documents réglementaires, tout en veillant au respect des protocoles d'étude et des exigences réglementaires applicables.
+ Collaborer avec les équipes multidisciplinaires afin de soutenir les opérations des essais cliniques et de résoudre les problèmes pouvant survenir au cours des études.
+ Assurer le suivi de l'avancement des essais, notamment en gérant les communications avec les sites investigateurs et en veillant à la livraison des matériels d'étude dans les délais requis.
+ Développer et maintenir des relations de travail solides avec le personnel des sites et les autres parties prenantes afin de favoriser le bon déroulement des opérations et la réussite globale des projets.
**Votre profil**
Vous possédez une solide expérience en soutien à la gestion des essais cliniques et êtes capable de travailler de façon autonome tout en accompagnant et en guidant vos collègues lorsque nécessaire.
**Qualifications et expérience requises :**
+ Diplôme universitaire (Licence/Bachelor ou équivalent) dans une discipline scientifique pertinente ou un domaine lié à la santé.
+ Expérience significative dans un rôle de soutien aux essais cliniques, avec une excellente compréhension des processus de recherche clinique et des exigences réglementaires.
+ Excellentes compétences organisationnelles et de gestion des priorités, avec la capacité de gérer efficacement plusieurs tâches et projets simultanément.
+ Maîtrise des systèmes de gestion des essais cliniques (CTMS) et des logiciels pertinents, avec une grande rigueur dans la gestion documentaire et des données.
+ Excellentes compétences en communication, en relations interpersonnelles et en résolution de problèmes, avec une capacité démontrée à collaborer efficacement avec des équipes et des intervenants variés.
+ Disponibilité pour des déplacements professionnels occasionnels (environ **10 % du temps** ).
**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

Clinical Trial Coordinator - Finance - Montreal, Canada
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:**
**Trial and site administration:**
+ Tracking (e.g. essential documents) and reporting (e.g, Safety Reports)
+ Ensure collation and distribution of study tools and documents
+ Update clinical trial databases (CTMS) and trackers
+ Clinical supply & non-clinical supply management, in Collaboration with other country roles
+ Manage Labeling requirements and coordinate/sign translation change request
**Document management:**
+ Prepare documents and correspondence
+ Collate, distribute/ship, and archive clinical documents
+ Assist with eTMF reconciliation
+ Updating manuals/documents (e.g., patient diaries, instructions)
+ Document proper destruction of clinical supplies.
+ Prepare Investigator trial file binders
+ Execute eTMF Quality Control Plan
+ Obtain translations of documents
**Regulatory & Site Start-Up responsibilities:**
+ In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start-up and submissions
+ Obtain, track and update study insurance certificates
+ Support preparation of submission package for IRB/ERC and support regulatory agencies submissions.
+ Publish study results for GCTO and RA where required per local legislation
**Budgeting, Agreement and Payments: Collaborate with finance/budgeting representatives for**
+ Develop country and site budgets (including Split site budget)
+ Tracking, and reporting of negotiations
+ Maintenance of tracking tools
+ Contract development, negotiation, approval and maintenance (e.g. CTRAs)
+ Update and maintain contract; templates (in cooperation with Legal Department)
+ Payment calculation and execution (investigators, vendors, grants)
+ Ensure compliance with financial procedures
+ Monitor and track adherence and disclosures,
+ Budget closeout.
**Meeting Planning:**
+ Organize meetings (create & track study memos/letters/protocols)
+ Support local investigator meetings (invitations, prepare materials, select venue, support vendor where applicable)
**What you need to have:**
+ B.A./B.S. (Life Science preferred) or equivalent healthcare experience
+ Minimum 1-2 years in Clinical Research or relevant healthcare experience
+ Must have at least 2 years of budget negotiation experience.
+ Fluent in Local Languages and business proficient in English (verbal and written} and excellent communication skills
+ Must be bilingual in French
+ Good understanding of Global; Country/Regional Clinical Research Guidelines and ability to work within these guidelines.
+ Hands on knowledge of Good Documentation Practices
+ Good IT skills (Use of MS office, use of some clinical IT applications on computer) and ability to adapt to new IT applications; Strong MS Excel skills required.
+ ICH-GCP Knowledge appropriate to role
+ Effective time management, organizational and interpersonal skills, conflict management
+ Effective communication with external customers (e.g. sites and investigators)
+ High sense of accountability/ urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment
+ Works effectively in a matrix multicultural environment. Ability to establish and maintain culturally sensitive working relationships.
+ Demonstrates commitment to Customer focus.
+ Able to work independently
+ Proactive attitude to solving problems/ proposing solution
+ Must be able to go on site to sponsor office 2 days a week in Kirkland
+ Eligible to work in Canada without visa sponsorship
**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

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first - developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.
**A Day in the Life**
Covering Vancouver
Responsibilities may include the following and other duties may be assigned.
+ Conducts on-site education and / or consulting.
+ Supports field personnel in providing the best possible outcomes and service for Medtronic customers.
+ Partners with sales colleagues to develop and execute plans of sales for within one or more business unit(s).
+ Participates in conventions, forums, and meetings to increase product awareness.
+ Works closely with Clinical Lead, Clinical Management and Regional Sales team to provide customer case and sales support.
+ Identifies and facilitates execution on growth opportunities with Sales and Clinical Support Team.
+ Serves as a technical resource to support sales of a specific medical product or solution.
**Salary Range: $78,720 - $98,400**
**PLEASE NOTE:**
+ We use artificial intelligence (AI) to review resumes of candidates and assess their fit based on the criteria outlined in the job posting. We do not use AI to make any final hiring or interview decisions.
+ This posting reflects a current, genuine vacancy that we are actively recruiting to fill.
**PHYSICAL JOB REQUIREMENTS**
+ _The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer and communicate with peers and co-workers._
Medtronic Canada strives through our vision to build a culture of inclusiveness through our commitment to employment equity and diversity. Discrimination is prohibited on any grounds protected under Canadian Human Rights legislation. Employment applications are encouraged from all members of our community. Upon request, candidates with disabilities will be accommodated during the recruitment process.
**SPECIALIST CAREER STREAM:** Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects - from design to implementation - while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education.
**DIFFERENTIATING FACTORS**
**Autonomy:** Established and productive individual contributor.
Works independently with general supervision on larger, moderately complex projects / assignments.
**Organizational Impact:** Sets objectives for own job area to meet the objectives of projects and assignments.
Contributes to the completion of project milestones .
May have some involvement in cross functional assignments.
**Innovation and Complexity:** Problems and issues faced are general, and may require understanding of broader set of issues or other job areas but typically are not complex .
Makes adjustments or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area.
**Communication and Influence:** Communicates primarily and frequently with internal contacts .
External interactions are less complex or problem solving in nature.
Contacts others to share information, status, needs and issues in order to inform, gain input, and support decision-making.
**Leadership and Talent Management:** May provide guidance and assistance to entry level professionals and / or employee in Support Career Stream.
**Required Knowledge and Experience:** Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education combined with experience.
Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)( 4)(iii)(A) and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience.
In the APAC Region Only:
- High School Diploma with a minimum of 6 years relevant experience; or
- Associate Diploma with a minimum of 4 years relevant experience
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. 

**Recruitment Fraud Alert**
We are aware of phishing scams targeting job seekers. Please keep the following in mind:
Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.
If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.
If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at .

**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email
To request removal of your personal information from our systems please email

Local Trial Manager - Oncology/Multi TA - Canada
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:**
The LTM role will be accountable/responsible for ensuring top-quality end-to-end trial delivery at a country level, managing the consistency of Local Trial Management duties and processes. The LTM will serve as the country-level single point of contact on the study for internal partners. While the LTM may delegate tasks to other LTMs or roles on the study, the LTM remains accountable for successful completion of those tasks.
The LTM will manage and oversee the following throughout the study:
+ Central IRB and other local vendors (Greenphire, Drug Destruction services, etc.) including set up of vendor purchase orders, invoice review and approval, and change-orders, as applicable.
+ Execution of local milestones from feasibility through study close out.
+ Resourcing of country-level roles, including support with transitions, in collaboration and agreement with the study Functional Manager (FM).
+ Inspection Readiness and AQR at the country level.
+ Close collaboration with the assigned Local Trial Manager(s) (LTMs), Lead Site Manager (LSM), Site Managers (SMs), Clinical Trial Associates (CTAs), and Site Contract Managers (SCMs) to outline accountabilities/responsibilities and provide support and training, where necessary.
+ Efficient communication with the Clinical Trial Managers (CTMs), Clinical Operations and the Global Trial Leader (GTL) to oversee trial excellence.
+ Country level ad hoc meetings during any phase of the study that are needed to address unexpected circumstances that might impact country or study level deliverables.
+ Close partnership with the study FM to provide updates, discuss hurdles, timelines/resources, and potential risks, and assist with documentation, such as storyboards, lessons-learned, metrics, etc., that may be required by leadership.
**What you need to have**
+ BA/BS degree.
+ Degree in a health or science related field.
+ 2 years of local trial management experience requied.
+ Start-up & Database Locks/Cleaning experience preferred
+ Cross therapeutic area trial management experience required.
+ Oncology trial management experience required, Early Development experience an asset.
+ Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations (i.e. Canadian), REB submissions, assigned protocols and associated protocol specific procedures.
+ Strong IT skills in appropriate software and company systems.
+ Willingness to travel with occasional overnight stay away from home according to business needs.
+ Proficient in speaking and writing the country language and English. Good written and oral communication skills as appropriate
+ To qualify, applicants must be legally authorized to work in Canada and should not require, now or in the future, sponsorship for employment visa status
**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

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Laboratory Setting, Office
**Job Description**
As part of the Thermo Fisher Scientific team, you'll 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 world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
We seek a Clinical Specialist to support growth through technical sales expertise and customer relationship management. Our Clinical Specialists are actively involved with Clinical Account activity, Strategic Sales Strategies, Business Development, Contract Implementation and Business Reviews. Working closely with sales teams and customers, you'll deliver effective value propositions, conduct product demonstrations, and provide comprehensive application support. Your role is essential in helping customers advance their research and support laboratory medicine while contributing to our mission of making the world healthier, cleaner, and safer.
REQUIREMENTS:
- Registered Medical Laboratory Technologist (MLT) or Bachelor of Medical Laboratory Science (BMLS) or Bachelor of Science (BSc) with appropriate major required
- MSc or PhD is an asset
- Deep technical expertise in relevant scientific applications and workflows
- Strong presentation and consultation skills for delivering technical product demonstrations
- Excellent verbal and written communication abilities in English; additional languages as needed
- Consistent record of meeting or exceeding sales targets
- Proficiency with CRM systems, Microsoft Office, and relevant technical software
- Strong project management and organizational capabilities
- Ability to travel 30-50% of time to customer sites and events
- Experience developing and maintaining strategic customer relationships
- In-depth knowledge of market trends, competitive landscape, and industry developments
- Ability to work effectively in a matrix organization
- Self-directed with ability to work independently while supporting team objectives
- Demonstrated problem-solving skills and technical troubleshooting abilities
- Commitment to continuous learning and staying current with scientific advances
**Compensation**
The estimated annualized pay range for this position in Ontario is $62,300.00-$83,000.00.
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.