Advance your clinical research career with Parexel as a Clinical Research Associate. Join a team that prioritizes patient care and site success with a focus on flexibility and qualified growth. In your role at Parexel, you will manage relationships and ensure the success of clinical sites.

Your responsibilities will include conducting visits such as qualification and monitoring, addressing site questions, and ensuring adherence to protocols. Parexel provides you with world-class resources, reduced travel, and prospects across therapeutic areas to enhance your expertise. Key Responsibilities:
Conduct qualification, initiation, monitoring, and termination visits
Oversee study integrity and foster site relationships
Safeguard patient rights throughout clinical trials




Develop patient recruitment strategies and meet enrollment timelines
Evaluate data quality, site efficacy, and drug accountability Requirements:
18+ months of onsite monitoring experience as a CRA
Bachelor’s degree in biological science, pharmacy, or health-related discipline
Excellent communication skills within a matrixed team
Self-driven with urgent project handling ability
Proficient in Clinical Trial Management Systems and MS-Office Leverage your monitoring skills and interpersonal abilities to make a difference in clinical research at Parexel.

📌 Clinical Research Associate At Parexel Mississauga
🏢 Parexel
📍 Mississauga