Clinical site monitoring expertise drives this remote Clinical Research Associate position at Parexel, supporting study quality, patient protection, and site relationships.

As a Clinical Research Associate, you will manage assigned sites from identification through close-out. You will serve as the sites’ sole contact, resolve questions, and oversee delivery. The work includes qualification, initiation, monitoring, and termination visits, alongside report generation and document verification.

Key Responsibilities:

- Conduct qualification, initiation, monitoring, and termination visits
- Generate visit and contact reports for assigned clinical sites
- Build site relationships and resolve study issues
- Safeguard human subjects’ rights and well-being




- Evaluate reported data, site efficacy, and drug accountability

Requirements:

- At least 18 months’ direct onsite monitoring experience
- Bachelor’s or equivalent degree in a health-related discipline
- Solid interpersonal, written, and verbal communication skills
- Knowledge of CTMS, EDMS, Excel, and Word
- Ability to manage multiple tasks and timelines independently

Apply clinical monitoring, communication, and quality expertise to support compliant research sites and patients through Parexel studies.

📌 Clinical Research Associate Site Monitor (Canada)
🏢 Parexel
📍 Canada