Senior Clinical Research Associate

Independent on-site monitoring experience

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

For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future.

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

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

Support regulatory team in preparing documents for study submissions

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 new medicines to those who need them.