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.
We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:
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.
Senior Clinical Research Associates train and coordinate junior CRAs while managing complex clinical studies, conducting site monitoring visits, and supporting investigators and study teams throughout trial progress.
Conduct clinical trial monitoring and site management across onsite and remote visits, taking ownership of study delivery, site performance, and quality while supporting strong site relationships.
Lead clinical study monitoring across Phase II and/or III trials, managing site relationships, study timelines, data quality, and compliance while supporting startup and regulatory submissions.
Independently oversee clinical trial monitoring from site initiation through close-out, maintaining GCP and regulatory compliance, strong investigator relationships, data quality, and trial integrity.
Monitor clinical trials across therapeutic areas, serving as the primary link between study teams, sponsors, and sites while ensuring site-level quality, compliance, data integrity, and study timelines.
