Contract Clinical Research Associate
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About the role
Contract remote Clinical Research Associate role for a candidate located in Canada’s West Coast. Responsibilities include site selection, initiation, monitoring and close-out visits; source data verification; investigational product accountability; document and TMF/ISF reconciliation; audit preparation; site training; and regulatory and ethics submission support. Requires 5+ years of independent on-site monitoring, phase I–III experience, and independent Oncology and Gastroenterology (IBD) trial monitoring, with travel up to 75%.
Key requirements
- • College/University degree in Life Sciences or an equivalent combination of education, training & experience
- • At least 5 years of relevant experience
- • Required skills: Independent on-site monitoring experience, Monitoring visits in phases I–III, Independent monitoring of Oncology clinical trials, Independent monitoring of Gastroenterology (IBD) clinical trials, MS Office applications, Planning and multitasking, Communication, Collaboration, Problem-solving, Ability to travel up to 75%
- • Professional registration/licence (Canada)
Opportunity details
- • Workplace: Remote
- • Employment: Contract
- • Posted: Nov 4, 2026
- • Original advert language: English
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Job title: Contract Clinical Research Associate