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 visitsPerform CRF review and source document verificationManage site communications effectivelyAct as a liaison for support services and vendorsParticipate in feasibility research and auditsRequirements:Degree in Life Sciences or equivalent experienceProven experience in Phase II and/or III monitoringExperience in Oncology is an assetBilingual proficiency in English and FrenchValid driver's license and willingness to travelElevate your clinical research expertise working with a dedicated team on life-changing studies.#J-18808-Ljbffr

📌 Freelance Senior Clinical Research Associate (Toronto)
🏢 PSI CRO
📍 Toronto