Elevate clinical trials with Parexel as a Clinical Research Associate II, managing sites and ensuring patient safety. This role includes travel and site monitoring across study phases.

As a Clinical Research Associate II, you will oversee site management, monitoring, and close-out activities for clinical trials. You will support investigator sites in compliance with Valuable Clinical Practices (GCP) and the Sponsor's standards. Your knowledge in clinical trial methodologies and previous monitoring experience will be key in facilitating effective communication and quality delivery throughout the trial.

Key Responsibilities:
• Manage site activation through database lock
• Serve as primary contact for assigned investigator sites




• Monitor adverse events and ensure reporting compliance
• Conduct remote/electronic monitoring as needed
• Submit required reports within specified timeframes

Requirements:
• Minimum 2 years of clinical research site monitoring experience
• Bachelor’s degree in life sciences or equivalent
• Fluent in English and local languages
• Ability to travel 60-80% for site visits
• Valid driver’s license and passport required

Utilize your monitoring experience and clinical knowledge to contribute to successful trials at Parexel.
#J-18808-Ljbffr

📌 Clinical Research Associate Remote (Newfoundland and Labrador)
🏢 Parexel
📍 Newfoundland and Labrador