Clinical trial monitoring and GCP compliance anchor this remote CRA opportunity with Parexel, focused on reliable data and protected participants.

Parexel’s Clinical Research Associate manages site quality and delivery across the study lifecycle. You will review trial performance, support enrollment strategies, and ensure compliance with protocols, SOPs, GCP, and regulations. The position combines site oversight, regulatory documentation, and client-focused communication.

Key Responsibilities:

- Review trial performance at designated clinical sites
- Develop recruitment strategies with clinical site teams
- Ensure protocol, SOP, GCP, and regulatory compliance
- Monitor regulatory documentation completeness and quality




- Perform site document verification and generate reports

Requirements:

- 18+ months of direct onsite CRA monitoring experience
- Degree in biological science, pharmacy, or related health discipline
- Strong written, verbal, and interpersonal communication abilities
- Self-driven approach with urgency and limited oversight
- Honest, ethical, adaptable, and client-focused work approach

Bring monitoring discipline, recruitment knowledge, and GCP understanding to help Parexel deliver quality clinical research outcomes.

📌 Clinical Trial Monitoring Associate (Canada)
🏢 Parexel
📍 Canada