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 opportunities 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.
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📌 Clinical Research Associate at Parexel (Manitoba)
🏢 Parexel
📍 Manitoba