As of November 6, 2026, Jobsy lists 22 clinical research associate jobs in Canada. The median advertised pay is $105,997 a year (from 9 postings). The most active employers are ICR Canada - CAN, PSI CRO and AbbVie. Skills often requested: clinical research, communication skills, google cloud and regulatory compliance.
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AbbVie
2+ YOECandidates need at least 2 years of clinically related monitoring experience, including on-site monitoring of investigational drug or device trials. They also need in-depth knowledge of GCP, ICH guidelines and clinical research regulations, plus strong organization and communication skills.
Microsoft Outlook, Microsoft PowerPoint, Microsoft Excel, Microsoft Word
AbbVie
2+ YOECandidates need at least 2 years of clinical monitoring experience, including on-site monitoring of investigational drug or device trials. They need in-depth knowledge of clinical research regulations and ICH/GCP guidelines, strong organizational and communication skills, and comfort with Microsoft Office and technology.
Microsoft Outlook, Microsoft PowerPoint, Microsoft Excel, Microsoft Word
AbbVie
2+ YOECandidates need at least 2 years of clinical monitoring experience, including on-site monitoring of investigational drug or device trials. They need in-depth knowledge of clinical research regulations and ICH/GCP guidelines, strong organizational and communication skills, and comfort with Microsoft Office and technology.
Microsoft Outlook, Microsoft PowerPoint, Microsoft Excel, Microsoft Word
AbbVie
1+ YOECandidates need at least one year of clinically related experience, including six months in clinical research monitoring of investigational drug or device trials. A health-related tertiary qualification is preferred, along with knowledge of ICH/GCP guidelines and strong cross-functional communication skills.
CRM tool
PSI CRO
5+ YOECandidates need a life sciences degree or equivalent, 5+ years of independent on-site monitoring experience across phases I-III, and independent oncology and IBD trial experience. They must live on Canada's West Coast, travel up to 75%, and hold a valid driver's licence.
MS Office
PSI CRO
Candidates need a university degree in Life Sciences or equivalent experience, independent onsite monitoring experience in North America, and experience with Phase II or III monitoring visits. Full working proficiency in English and French and travel ability are also required.
MS Office
PSI CRO
Candidates need a college or university degree in life sciences or equivalent experience, plus independent onsite monitoring experience in Phase II and/or III trials. Full English proficiency, MS Office skills, travel ability and a valid driver's licence are required.
MS Office
PSI CRO
Candidates need a life sciences degree or equivalent experience, independent onsite monitoring experience in Phase II or III studies, and full working proficiency in English and French. Travel and a valid driver's licence are required.
MS Office
Novo Nordisk
5+ YOECandidates need a bachelor's degree in life sciences or a related field and 5+ years of CRA experience. They must know ICH-GCP, use clinical trial systems such as EDC, CTMS and eTMF, and be able to travel up to 70% of the time.
EDC, CTMS, eTMF
Medpace, Inc.
2+ YOECandidates need a life science bachelor's degree and at least 2 years as a Clinical Research Coordinator. They must be bilingual in English and French and know ICH E-6 and Health Canada clinical trial regulations.
Microsoft Office, CTMS
adecco
2+ YOECandidates need at least 2 years of experience conducting clinical studies and knowledge of clinical research regulations and quality standards. A science bachelor's degree is preferred, and experience with medical devices, diagnostics or Veeva TMF is an asset. Candidates must be legally eligible to work and reside in Canada.
Veeva
Profound Medical: (NASDAQ:PROF) is a commercial-stage medical technology company based in Mississauga, Ontario, advancing the standard of care for prostate cancer and…
1+ YOECandidates need a bachelor's degree in biomedical sciences, ideally an MSc or research experience, and 1-3 years of clinical trial experience. They must know GCP, ethics and regulatory requirements, and communicate clearly while travelling up to 60% of the time.
Clinical research, Analyse issues, Monitor activities, Documentation, Inspection, Improve business processes
Syneos Health, LLC
Candidates need a bachelor's degree or RN in a related field, or equivalent experience. They need knowledge of GCP/ICH guidelines, good computer skills, strong communication skills and the ability to travel up to 75%.
Electronic data capture systems, Trial Master File, Clinical data tracking systems
Syneos Health, LLC
Candidates need fluency in both French and English, plus clinical monitoring experience and a working knowledge of ICH-GCP, relevant regulations and company SOPs. Strong judgment, adaptability to changing priorities and comfort with electronic data capture systems are expected.
Electronic data capture systems, Tracking systems, Case report forms
The median advertised pay is $105,997 a year, across 9 postings that list pay. The lowest quarter pays under $105,997 and the top quarter over $110,510.
ICR Canada - CAN (5), PSI CRO (4), AbbVie (4), Syneos Health, LLC (2) and Novo Nordisk (1).
Postings most often mention clinical research, communication skills, google cloud, regulatory compliance, clinical trials, problem solving, reporting and collaboration.
11 companies