Use independent monitoring expertise as a Senior Clinical Research Associate supporting clinical studies across Canada. Apply solid communication and site management skills.

PSI seeks an experienced freelance Senior Clinical Research Associate for Phase II and/or III studies. The work includes onsite monitoring, CRF review, source document verification, query resolution, and communication with project teams. Oncology experience is a plus.

Key Responsibilities:

- Conduct and report SIV, RMV, and COV onsite monitoring visits
- Perform CRF review and source document verification
- Resolve queries and manage site communication
- Coordinate with internal support services and vendors
- Support feasibility research, submissions, audits, and inspections

Requirements:

- College or university degree in Life Sciences or equivalent experience
- Independent onsite monitoring experience
- Phase II and/or III monitoring visit experience
- Full working proficiency in English and MS Office
- Ability to travel with a valid driver’s license

Bring clinical monitoring, site management, and communication expertise to PSI’s freelance research work across Canada.

📌 Senior Clinical Research Associate Canada
🏢 PSI CRO
📍 Canada