Join a global leader in clinical research as a Freelance Senior Clinical Research Associate. This role focuses on monitoring and supporting cutting-edge medical studies across Canada.
We're seeking an experienced CRA to conduct onsite monitoring visits and ensure compliance with study protocols. You will play a critical role in site management and communication, supporting both the regulatory team and internal project groups. This position is well-suited for candidates with expertise in Phase II and III monitoring.
Key Responsibilities: • Conduct and report site initiation, monitoring, and close-out visits • Perform CRF review and source document verification • Manage site communications effectively • Act as a liaison for support services and vendors • Participate in feasibility research and audits
Requirements: • Degree in Life Sciences or equivalent experience • Proven experience in Phase II and/or III monitoring • Experience in Oncology is an asset • Bilingual proficiency in English and French • Valid driver’s license and willingness to travel
Elevate your clinical research expertise working with a dedicated team on life-changing studies. #J-18808-Ljbffr