Monitor clinical trials with Pharma Medica Research in Scarborough, applying Good Clinical Practice and regulatory compliance expertise across clinical sites. Travel is required.

The Senior Clinical Research Associate monitors trials at PMRI’s facility and external sites. Reporting to project management, this position acts for Sponsors, protecting subjects and supporting compliant research. The work requires careful documentation, site communication, and corrective-action follow-up.

Key Responsibilities:

- Monitor trials for GCP, protocol, SOP, and regulatory compliance
- Perform initiation, pre-study, on-study, and close-out visits
- Review source documents and verify CRF transcription accuracy
- Document visits and follow up on corrective actions
- Communicate observations with sites and Sponsors promptly

Requirements:

- Bachelor of Sciences degree
- Additional clinical research education and training
- Five years of CRA experience in a CRO
- Excellent GCP knowledge and communication skills
- Ability to travel and work with minimum supervision

Apply clinical monitoring, GCP knowledge, and transparent communication to support compliant trials at PMRI’s Scarborough sites.

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📌 Senior Clinical Research Associate (Toronto)
🏢 Pharma Medica Research
📍 Toronto