Parexel’s remote Clinical Research Associate role centers on regulatory quality, patient safety, and robust clinical site partnerships.

You will act as the primary contact for assigned sites while maintaining study integrity and delivery. Responsibilities span site visits, issue resolution, patient recruitment, data quality, drug accountability, and regulatory documentation. Parexel provides technology and training tailored to individual experience, with opportunities across therapeutic areas.

Key Responsibilities:

- Oversee study integrity and promote site rapport
- Address and resolve site questions and issues
- Protect patient rights and well-being according to protocol
- Assess data quality, site efficacy, and drug accountability




- Complete regulatory document checks and verification activities

Requirements:

- 18+ months’ onsite monitoring experience as a CRA
- Bachelor’s or equivalent degree in biological or health sciences
- Ability to manage unpredictable scenarios and project timelines
- Strong computer skills with CTMS, EDMS, Excel, and Word
- Understanding of study protocols within matrixed teams

Use ethical judgment, regulatory knowledge, and site management skills to advance quality research delivery with Parexel.

📌 Clinical Research Associate Regulatory Quality (Canada)
🏢 Parexel
📍 Canada