Your expertise is needed as a Senior Clinical Research Associate in Canada! This freelance role focuses on site monitoring and regulatory support in a dynamic healthcare environment.

This position requires a seasoned professional to conduct site initiation, monitoring visits, and prepare for inspections. You will collaborate closely with internal teams while managing communication with study sites. Candidates with experience in Oncology will find this role especially rewarding.

Key Responsibilities: • Conduct and report on-site monitoring visits as required • Review CRFs and verify source documents for accuracy • Facilitate communications among project teams and sites • Participate in audits and regulatory document preparation • Support feasibility studies for upcoming trials

Requirements: • Bachelor's degree in Life Sciences or similar field • Experience with Phase II and III monitoring visits • Bilingual proficiency in English and French • Robust communication and problem-solving skills • Valid driver’s license and ability to travel

Expand your clinical research skills while impacting lives in Canada’s healthcare landscape. #J-18808-Ljbffr

📌 Senior Clinical Research Associate in Canada (Winnipeg)
🏢 PSI CRO
📍 Winnipeg