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Clinical trial manager Jobs in Montreal, QC
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Clinical trial manager • montreal qc
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Clinical Project Manager
Keyrus Life Science North AmericaMount Royal, Montreal (administrative region), Canada- Promoted
CANTRAIN’s Designer & Developer of Clinical Trial Training Programs (Research Institute)
McGill University Health CentreMontreal, Montreal (administrative region), CanadaClinical Research Coordinator - Nurse (Research Institute)
Research Institute of the McGill University Health CentreMontréal, CA- Promoted
Clinical Research Associate - Oncology - Sponsor Dedicated - Montreal or Quebec City
ICON Strategic SolutionsGreater Montreal Metropolitan Area, Canada- Promoted
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Clinical Data Manager (Canada)
Indero (anciennement Innovaderm)Montreal, Montreal (administrative region), Canada- Promoted
Clinical Operations Specialist
Syneos Health, Inc.Montreal, Montreal (administrative region), Canada- Promoted
Clinical Investigator (MD)
AltasciencesMontreal, Montreal (administrative region), Canada- Promoted
Site Budget & Proposal Manager / Gestionnaire des budgets et des propositions
Indero (formerly Innovaderm)Montreal, Montreal (administrative region), Canada- Promoted
Specialized Nurse Practitioner
Altasciences Co.Laval, QC, Canada- Promoted
CSC Digital Portfolio Manager / Project Manager - Full remote (F / M)
ALSINOVA CROMontreal, Montreal (administrative region), Canada- Promoted
Experienced Clinical Research Associate (CRA II / Senior / PCRA) - Bilingual - Montreal, Quebec
Thermo Fisher Scientific Inc.Montreal, Montreal (administrative region), Canada- Promoted
Experienced Clinical Research Associate (CRA II / Senior / PCRA) - Bilingual - Montreal, Quebec
Thermo Fisher ScientificMontreal, Montreal (administrative region), Canada- Promoted
Manager, Clinical Operations
AbbVieMontreal, QC, Canada- Promoted
Manager, Oncology Clinical Research Unit (Research Institute)
RI-MUHC | Research Institute of the MUHC | #rimuhcMontreal, Montreal (administrative region), Canada- Promoted
Clinical Trial Assistant (CTA)
IQVIAMontreal, Montreal (administrative region), Canada- Promoted
Clinical Trial Manager II / Gestionnaire d'essais cliniques II, Dermatology & Rheumatology, Canada
InderoMontreal, QC, Canada- Promoted
Manager, Clinical Operations
AllerganMontreal, Montreal (administrative region), Canada- Promoted
Director of Nursing, Clinical Trials & Real-World Delivery
Famililab.CareMontreal, QC, Canada- Promoted
Manager, Clinical Operations
AbbVie IncMontreal, Montreal (administrative region), Canada- Promoted
Clinical Research Coordinator – Entry Position (Research Institute)
IR-CUSM | Institut de recherche du CUSM | #ircusmMontreal, Montreal (administrative region), Canada- Vancouver, BC (from $ 90,660 to $ 199,800 year)
- Bradford West Gwillimbury, ON (from $ 112,621 to $ 199,800 year)
- Mississauga, ON (from $ 164,500 to $ 199,262 year)
- Old toronto, ON (from $ 107,655 to $ 196,000 year)
- Toronto, ON (from $ 109,985 to $ 195,808 year)
- Winnipeg, MB (from $ 55,662 to $ 195,062 year)
- Montreal-Ouest, QC (from $ 75,712 to $ 173,203 year)
- Montreal, QC (from $ 75,712 to $ 173,203 year)
- Edmonton, AB (from $ 101,888 to $ 134,550 year)
- Hamilton, ON (from $ 92,459 to $ 95,818 year)
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Clinical Project Manager
Keyrus Life Science North AmericaMount Royal, Montreal (administrative region), Canada- Full-time
The Clinical Project Manager (CPM) plays a crucial role in advancing the progress of clinical trials. Join this emerging team in Canada with our client and enhance your career potential. Be part of a fast-growing, dynamic biotech company.
The Clinical Project Manager is an experienced professional in clinical research and healthcare management. Their responsibilities include managing and coordinating various aspects of clinical trials. Key duties and responsibilities include :
- Strategic Planning :
Develop comprehensive plans for initiating, executing, and completing clinical trials, aligning with project goals and timelines.
Contribute to creating and refining study protocols, outlining methodology, objectives, ICF, eCRF, and other study-related documents.
Identify and manage risks associated with clinical trials and make recommendations.
Collaborate with the European Clinical Head and local support. Supervise clinical research associates and documentation specialists.
Manage vendors to ensure patient safety, contract adherence, data integrity, and financial engagement.
Prepare and review documents related to clinical projects (contracts, vendor budgets, reports).
Participate in data analysis, summarization, and reporting for regulatory purposes.
Master's degree in a scientific discipline (biology, biomedical sciences, pharmacy) or equivalent.
Salary based on experience plus benefits, including RRSP matching.
Keyrus Life Science is an international CRO and consulting organization committed to transparency, integrity, and excellence. We focus on delivering high-quality services across various stages of drug development, including project management, clinical operations, pharmacovigilance, and more.
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