We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing current medicines to those who need them.

We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada: Conduct and report SIV, RMV, COV onsite monitoring visits

Perform CRF review, source document verification and query resolution

Be responsible for site communication and management

Be a point of contact for in-house support services and vendors

Communicate with internal project teams regarding study progress

Participate in feasibility research

Support regulatory team in preparing documents for study submissions





Prepare and particiapte on audits and inspections Qualifications College/University degree in Life Sciences or an equivalent combination of education, training & experience

Independent on-site monitoring experience

Experience in all types of monitoring visits in Phase II and/or III

Experience in Oncology is a plus

Full working proficiency in English. Proficiency in MS Office applications

Ability to plan, multitask and work in a dynamic team environment

Communication, collaboration, and problem-solving skills

Ability to travel

Valid driver’s license Additional Information This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

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