56 Medical Researchers jobs in Canada
Scientific Research and Experimental Development (SR&ED) Intern
Toronto, Ontario
Stantec
Posted 2 days ago
Job Viewed
Job Description
At Stantec, we have some of the world's leading professionals passionate about enabling our business to be its best. Our business teams include finance, procurement, human resources, information technology, marketing, corporate development, HSSE, real estate, legal, and practice services. We bring diverse backgrounds, skills, and expertise and create a caring culture where everyone can thrive. Through teamwork and collaboration, we're building a stronger, more resilient Stantec every day.
Your Opportunity
Stantec enhances its value to clients and shareholders by strengthening its technical capacity through scientific research and innovation. The Stantec Research Services team facilitates Stantec engagement in research by accessing research funding and other resources. One major source of funding is the Canadian federal government's research tax credit program "Scientific Research and Experimental Development" (SR&ED).
As the Scientific Research & Experimental Development (SR&ED) Intern, on Stantec's Research Services team, make a career-building move in which you can leverage your organizational skills while learning about and furthering innovative work at Stantec. You will join our global Innovation Office team, learning about some of the most innovative science and technology projects across Canada, and accessing government funding for those projects. This position will commence January 2026 and the term is expected to last six months. Stantec supports hybrid work arrangements where employees can work remotely or from the office, as needed, based on demands of specific tasks, work preferences, and operational requirements.
Your Key Responsibilities
- Work with Research Advisor (Canada) using your organizational skills to advance the annual cycle of SR&ED claim development at Stantec which includes:
- Planning - identify all necessary elements of claim development and schedule them
- Documenting - attend project calls, summarize information, group with similar claims
- Tracking - follow each lead from identification to completed claim, and record each step
- Supporting - Assist in gathering, reviewing, and organizing supporting documentation, as well as contributing to the cost estimation process.
- Monitoring - keep the claim process on schedule through structured reminders
- Provide support for other Stantec programs that address researchers' needs, in collaboration with the Manager of Research Services, as required.
Your Capabilities and Credentials
- Highly organized and skilled at working in a team environment on time-sensitive projects
- Excellent written and verbal communication skills
- Familiar with engineering and scientific language; able to understand engineering processes
- Ability to work effectively in an online environment, offering, and receiving information within specific timeframes.
Education and Experience
- Currently enrolled in a master's program in science or engineering.
- Demonstrated proficiency in Python programming is essential.
- Please confirm your availability for a six-month term beginning in January 2026.
Typical office or home office environment working with computers and remaining sedentary for long periods of time.
This description is not a comprehensive listing of activities, duties or responsibilities that may be required of the employee and other duties, responsibilities and activities may be assigned or may be changed at any time with or without notice.
Stantec is a place where the best and brightest come to build on each others' talents, do exciting work, and make an impact on the world around us. Join us and redefine your personal best.
**Pay Transparency:** In compliance with pay transparency laws, pay ranges are provided for positions in locations where required. Please note, the final agreed upon compensation is based on individual education, qualifications, experience, and work location. At Stantec certain roles are bonus eligible.
**Benefits Summary:** Regular full-time and part-time employees (working at least 20 hours per week) will have access to health, dental, and vision plans, a wellness program, health care spending account, wellness spending account, group registered retirement savings plan, employee stock purchase program, group tax-free savings account, life and accidental death & dismemberment (AD&D) insurance, short-term/long-term disability plans, emergency travel benefits, tuition reimbursement, professional membership fee coverage, and paid time off.
Temporary/casual employees will have access to group registered retirement savings plan, employee stock purchase program, and group tax-free savings account.
The benefits information listed above may not apply to union positions because benefits for such positions are governed by applicable collective bargaining agreements.
**Primary Location:** Canada | ON | Toronto
**Organization:** 1298 Innovation-CA-Toronto ON
**Employee Status:** Regular
**Travel:** No
**Schedule:** Full time
**Job Posting:** 09/10/ :10:14
**Req ID:**
Your Opportunity
Stantec enhances its value to clients and shareholders by strengthening its technical capacity through scientific research and innovation. The Stantec Research Services team facilitates Stantec engagement in research by accessing research funding and other resources. One major source of funding is the Canadian federal government's research tax credit program "Scientific Research and Experimental Development" (SR&ED).
As the Scientific Research & Experimental Development (SR&ED) Intern, on Stantec's Research Services team, make a career-building move in which you can leverage your organizational skills while learning about and furthering innovative work at Stantec. You will join our global Innovation Office team, learning about some of the most innovative science and technology projects across Canada, and accessing government funding for those projects. This position will commence January 2026 and the term is expected to last six months. Stantec supports hybrid work arrangements where employees can work remotely or from the office, as needed, based on demands of specific tasks, work preferences, and operational requirements.
Your Key Responsibilities
- Work with Research Advisor (Canada) using your organizational skills to advance the annual cycle of SR&ED claim development at Stantec which includes:
- Planning - identify all necessary elements of claim development and schedule them
- Documenting - attend project calls, summarize information, group with similar claims
- Tracking - follow each lead from identification to completed claim, and record each step
- Supporting - Assist in gathering, reviewing, and organizing supporting documentation, as well as contributing to the cost estimation process.
- Monitoring - keep the claim process on schedule through structured reminders
- Provide support for other Stantec programs that address researchers' needs, in collaboration with the Manager of Research Services, as required.
Your Capabilities and Credentials
- Highly organized and skilled at working in a team environment on time-sensitive projects
- Excellent written and verbal communication skills
- Familiar with engineering and scientific language; able to understand engineering processes
- Ability to work effectively in an online environment, offering, and receiving information within specific timeframes.
Education and Experience
- Currently enrolled in a master's program in science or engineering.
- Demonstrated proficiency in Python programming is essential.
- Please confirm your availability for a six-month term beginning in January 2026.
Typical office or home office environment working with computers and remaining sedentary for long periods of time.
This description is not a comprehensive listing of activities, duties or responsibilities that may be required of the employee and other duties, responsibilities and activities may be assigned or may be changed at any time with or without notice.
Stantec is a place where the best and brightest come to build on each others' talents, do exciting work, and make an impact on the world around us. Join us and redefine your personal best.
**Pay Transparency:** In compliance with pay transparency laws, pay ranges are provided for positions in locations where required. Please note, the final agreed upon compensation is based on individual education, qualifications, experience, and work location. At Stantec certain roles are bonus eligible.
**Benefits Summary:** Regular full-time and part-time employees (working at least 20 hours per week) will have access to health, dental, and vision plans, a wellness program, health care spending account, wellness spending account, group registered retirement savings plan, employee stock purchase program, group tax-free savings account, life and accidental death & dismemberment (AD&D) insurance, short-term/long-term disability plans, emergency travel benefits, tuition reimbursement, professional membership fee coverage, and paid time off.
Temporary/casual employees will have access to group registered retirement savings plan, employee stock purchase program, and group tax-free savings account.
The benefits information listed above may not apply to union positions because benefits for such positions are governed by applicable collective bargaining agreements.
**Primary Location:** Canada | ON | Toronto
**Organization:** 1298 Innovation-CA-Toronto ON
**Employee Status:** Regular
**Travel:** No
**Schedule:** Full time
**Job Posting:** 09/10/ :10:14
**Req ID:**
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Clinical Research Coordinator
Stoney Creek, New Brunswick
ClinSurge Research
Posted today
Job Viewed
Job Description
Job Description
Job Description
Position Summary:
We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to manage and coordinate clinical research studies in accordance with Good Clinical Practice (GCP), institutional guidelines, and federal regulations. The CRC will work closely with investigators, sponsors, and participants to ensure the integrity of study protocols and data collection.
Key Responsibilities:
- Coordinate and conduct all aspects of clinical research studies, including participant recruitment, consent, scheduling, and follow-up.
- Ensure compliance with study protocols and regulatory requirements (Health Canada, IRB, ICH-GCP).
- Collect and enter data accurately into electronic data capture (EDC) systems.
- Maintain study documents, including electronic regulatory binders, subject files, and case report forms.
- Monitor and report adverse events and ensure timely communication with the IRB and sponsors.
- Prepare for and participate in monitoring visits, audits, and inspections.
- Collaborate with cross-functional teams, including principal investigators, sponsors, and other research personnel.
Qualifications:
- Bachelor’s degree in health sciences, life sciences, nursing, or a related field (required).
- Minimum (1-3) years of experience in clinical research (preferred).
- Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) a plus.
- Phlebotomy certification and proficiency in drawing with ability to process and ship per IATA requirements.
- Strong knowledge of GCP, Health Canada, and IRB regulations.
- Excellent organizational, communication, and problem-solving skills.
- Proficiency with EDC systems (e.g., Medidata, or RAVE) and Microsoft Office Suite.
Work Environment:
- On-site in physician practice and clinical research setting.
- May require handling of biological samples and/or working with patients.
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1
Clinical Research Coordinator
Mississauga, Ontario
ClinSurge Research
Posted today
Job Viewed
Job Description
Job Description
Job Description
Position Summary:
We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to manage and coordinate clinical research studies in accordance with Good Clinical Practice (GCP), institutional guidelines, and federal regulations. The CRC will work closely with investigators, sponsors, and participants to ensure the integrity of study protocols and data collection.
Key Responsibilities:
- Coordinate and conduct all aspects of clinical research studies, including participant recruitment, consent, scheduling, and follow-up.
- Ensure compliance with study protocols and regulatory requirements (Health Canada, IRB, ICH-GCP).
- Collect and enter data accurately into electronic data capture (EDC) systems.
- Maintain study documents, including electronic regulatory binders, subject files, and case report forms.
- Monitor and report adverse events and ensure timely communication with the IRB and sponsors.
- Prepare for and participate in monitoring visits, audits, and inspections.
- Collaborate with cross-functional teams, including principal investigators, sponsors, and other research personnel.
Qualifications:
- Bachelor’s degree in health sciences, life sciences, nursing, or a related field (required).
- Minimum (1-3) years of experience in clinical research (preferred).
- Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) a plus.
- Phlebotomy certification and proficiency in drawing with ability to process and ship per IATA requirements.
- Strong knowledge of GCP, Health Canada, and IRB regulations.
- Excellent organizational, communication, and problem-solving skills.
- Proficiency with EDC systems (e.g., Medidata, or RAVE) and Microsoft Office Suite.
Work Environment:
- On-site in physician practice and clinical research setting.
- May require handling of biological samples and/or working with patients.
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2
Senior Clinical Research Associate
ICON Clinical Research
Posted 22 days ago
Job Viewed
Job Description
Clinical Research Associate, Toronto, Canada, Oncology Required
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 CRA you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.
En tant qu'ARC (Associé(e) de recherche clinique), vous rejoindrez la plus grande et la plus complète organisation de recherche clinique au monde, propulsée par l'intelligence en santé.
**What You Will Be Doing:**
+ Contribute to the identification of new sites for clinical trials
+ Assume ambassadorial role to facilitate communication between sites and sponsor CPO to increase value proposition to investigators.
+ Facilitate the preparation and collection of site and country level documents during all phases of the trial. Supports the Clinical Study Manager in the oversight of Country and Site Trial Master Files (TMF). During all phases of the trial ensure archiving per relevant SOP.
+ Execute site initiation and training, generate initiation visit report.
+ Implement complete site management including monitoring visits, regulatory assessment, drug supply management, etc. to ensure compliance with protocol, GCP, global and local regulations, global and local processes.
+ Identify problems at sites; resolve issues and escalate as appropriate.
+ Complete preparation and generation of visit monitoring reports as per relevant SOP.
+ Review and manage data at site; resolve technical and content issues on a continuous basis in order to achieve timely database lock targets.
+ Implement site close-out activities and generate site close-out report.
+ Provide feedback on site performance for future trial site feasibility/selection
+ Improve skills by timely completion performance of assigned global and local training.
+ **Responsabilités:**
+ Contribuer à l'identification de nouveaux centres pour des études cliniques
+ Assumer un rôle d'ambassadeur pour faciliter les communications entre les centres d'étude et le Directeur de l'expérience patient du promoteur, afin de rehausser la proposition de valeur aux chercheurs.
+ Faciliter la préparation et la collecte des documents aux centres d'étude et à l'échelle du pays pendant toutes les phases d'étude. Soutenir le travail du gestionnaire de l'étude clinique pour la surveillance des fichiers maîtres de l'étude (FME) aux centres d'étude et à l'échelle du pays. Pendant toutes les phases d'étude, s'assurer que l'archivage est conforme aux procédures d'exploitation normalisées.
+ Effectuer l'initiation des centres d'étude et la formation du personnel, rédiger le rapport de la visite d'initiation.
+ Mettre en place la structure complète de gestion des centres d'étude, entre autres, les visites de surveillance, les évaluations réglementaires, la gestion de l'approvisionnement en médicaments, pour assurer la conformité au protocole, aux BPC, aux réglementations mondiales et locales, et aux processus mondiaux et locaux.
+ Identifier les problèmes aux centres d'étude; résoudre les problèmes et les communiquer à un palier supérieur de la direction, le cas échéant.
+ Effectuer la rédaction complète et la distribution des rapports sur les visites de surveillance, conformément aux procédures d'exploitation normalisées pertinentes.
+ Examiner et gérer continuellement les données recueillies aux centres d'étude, afin de résoudre rapidement les problèmes techniques et de contenu pour atteindre les cibles de verrouillage de la base de données en temps opportun.
+ Mettre en œuvre les activités de clôture des centres d'étude et rédiger le rapport de clôture des centres d'étude.
+ Fournir des commentaires sur les performances des centres d'étude afin d'évaluer leur candidature pour de futures études cliniques.
**Your Profile:**
+ Bachelor's Degree or higher in life sciences or equivalent
+ Minimum 2 years' clinical site monitoring experience from CRO or Pharmaceutical company
+ Comprehensive knowledge and understanding of ICH-GCP
+ Able and willing to travel up to 60% regionally (sites in Quebec City and Montreal)
+ Able and willing to work on several protocols/therapy areas
+ Experience in phase I-IV trials
+ Working knowledge of Electronic Data Capture (preferred)
+ Experience/working knowledge of the oncology disease area (preferred but not required)
+ Experience of Centralized/Risk Based/Targeted monitoring (preferred)
+ Experience of working within a metric based environment (preferred)
+ Excellent attention to detail
+ Highly developed time management and organizational skills
+ Focused on meeting study deliverables/targets
+ Flexible and willing to adapt to changing priorities/timelines
+ Experience in oncology is required
+ Blingual English/French Required
**Compétences**
+ Baccalauréat ou diplôme supérieur en sciences de la vie ou un équivalent
+ Minimum de 2 à 4 ans d'expérience en surveillance de centres d'étude pour une entreprise de recherche contractuelle ou une société pharmaceutique
+ Des connaissances et une compréhension approfondies des bonnes pratiques cliniques élaborées par la Conférence internationale sur l'harmonisation (BPC-CIH)
+ Bilinguisme français/anglais (maîtrise verbale et écrite) exigé
+ Disposé(e) et apte à voyager jusqu'à 60 % du temps à l'échelle régionale (centres d'étude à Québec et à Montréal)
+ Disposé(e) et apte à travailler sur plusieurs protocoles/domaines thérapeutiques
+ Expérience dans les études cliniques de phase I à IV
+ Connaissance pratique de la saisie électronique des données (préférable)
+ Expérience/connaissance pratique dans le domaine des maladies oncologiques (préférable, mais non requise)
+ Expérience dans la surveillance centralisée/axée sur les risques/ciblée (préférable)
+ Expérience de travail dans un environnement métrique (préférable)
+ Souci du détail
+ Compétences organisationnelles et de gestion du temps de haut niveau
+ Déterminé(e) à fournir les livrables et atteindre les objectifs des études
+ Flexible et disposé(e) à s'adapter aux changements dans les priorités/échéanciers
**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.
As a CRA you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.
En tant qu'ARC (Associé(e) de recherche clinique), vous rejoindrez la plus grande et la plus complète organisation de recherche clinique au monde, propulsée par l'intelligence en santé.
**What You Will Be Doing:**
+ Contribute to the identification of new sites for clinical trials
+ Assume ambassadorial role to facilitate communication between sites and sponsor CPO to increase value proposition to investigators.
+ Facilitate the preparation and collection of site and country level documents during all phases of the trial. Supports the Clinical Study Manager in the oversight of Country and Site Trial Master Files (TMF). During all phases of the trial ensure archiving per relevant SOP.
+ Execute site initiation and training, generate initiation visit report.
+ Implement complete site management including monitoring visits, regulatory assessment, drug supply management, etc. to ensure compliance with protocol, GCP, global and local regulations, global and local processes.
+ Identify problems at sites; resolve issues and escalate as appropriate.
+ Complete preparation and generation of visit monitoring reports as per relevant SOP.
+ Review and manage data at site; resolve technical and content issues on a continuous basis in order to achieve timely database lock targets.
+ Implement site close-out activities and generate site close-out report.
+ Provide feedback on site performance for future trial site feasibility/selection
+ Improve skills by timely completion performance of assigned global and local training.
+ **Responsabilités:**
+ Contribuer à l'identification de nouveaux centres pour des études cliniques
+ Assumer un rôle d'ambassadeur pour faciliter les communications entre les centres d'étude et le Directeur de l'expérience patient du promoteur, afin de rehausser la proposition de valeur aux chercheurs.
+ Faciliter la préparation et la collecte des documents aux centres d'étude et à l'échelle du pays pendant toutes les phases d'étude. Soutenir le travail du gestionnaire de l'étude clinique pour la surveillance des fichiers maîtres de l'étude (FME) aux centres d'étude et à l'échelle du pays. Pendant toutes les phases d'étude, s'assurer que l'archivage est conforme aux procédures d'exploitation normalisées.
+ Effectuer l'initiation des centres d'étude et la formation du personnel, rédiger le rapport de la visite d'initiation.
+ Mettre en place la structure complète de gestion des centres d'étude, entre autres, les visites de surveillance, les évaluations réglementaires, la gestion de l'approvisionnement en médicaments, pour assurer la conformité au protocole, aux BPC, aux réglementations mondiales et locales, et aux processus mondiaux et locaux.
+ Identifier les problèmes aux centres d'étude; résoudre les problèmes et les communiquer à un palier supérieur de la direction, le cas échéant.
+ Effectuer la rédaction complète et la distribution des rapports sur les visites de surveillance, conformément aux procédures d'exploitation normalisées pertinentes.
+ Examiner et gérer continuellement les données recueillies aux centres d'étude, afin de résoudre rapidement les problèmes techniques et de contenu pour atteindre les cibles de verrouillage de la base de données en temps opportun.
+ Mettre en œuvre les activités de clôture des centres d'étude et rédiger le rapport de clôture des centres d'étude.
+ Fournir des commentaires sur les performances des centres d'étude afin d'évaluer leur candidature pour de futures études cliniques.
**Your Profile:**
+ Bachelor's Degree or higher in life sciences or equivalent
+ Minimum 2 years' clinical site monitoring experience from CRO or Pharmaceutical company
+ Comprehensive knowledge and understanding of ICH-GCP
+ Able and willing to travel up to 60% regionally (sites in Quebec City and Montreal)
+ Able and willing to work on several protocols/therapy areas
+ Experience in phase I-IV trials
+ Working knowledge of Electronic Data Capture (preferred)
+ Experience/working knowledge of the oncology disease area (preferred but not required)
+ Experience of Centralized/Risk Based/Targeted monitoring (preferred)
+ Experience of working within a metric based environment (preferred)
+ Excellent attention to detail
+ Highly developed time management and organizational skills
+ Focused on meeting study deliverables/targets
+ Flexible and willing to adapt to changing priorities/timelines
+ Experience in oncology is required
+ Blingual English/French Required
**Compétences**
+ Baccalauréat ou diplôme supérieur en sciences de la vie ou un équivalent
+ Minimum de 2 à 4 ans d'expérience en surveillance de centres d'étude pour une entreprise de recherche contractuelle ou une société pharmaceutique
+ Des connaissances et une compréhension approfondies des bonnes pratiques cliniques élaborées par la Conférence internationale sur l'harmonisation (BPC-CIH)
+ Bilinguisme français/anglais (maîtrise verbale et écrite) exigé
+ Disposé(e) et apte à voyager jusqu'à 60 % du temps à l'échelle régionale (centres d'étude à Québec et à Montréal)
+ Disposé(e) et apte à travailler sur plusieurs protocoles/domaines thérapeutiques
+ Expérience dans les études cliniques de phase I à IV
+ Connaissance pratique de la saisie électronique des données (préférable)
+ Expérience/connaissance pratique dans le domaine des maladies oncologiques (préférable, mais non requise)
+ Expérience dans la surveillance centralisée/axée sur les risques/ciblée (préférable)
+ Expérience de travail dans un environnement métrique (préférable)
+ Souci du détail
+ Compétences organisationnelles et de gestion du temps de haut niveau
+ Déterminé(e) à fournir les livrables et atteindre les objectifs des études
+ Flexible et disposé(e) à s'adapter aux changements dans les priorités/échéanciers
**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.
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