Advance your career at Parexel as a Clinical Research Associate II, responsible for managing clinical trial sites and ensuring compliance. This position includes regular travel and site engagement.

In this Clinical Research Associate II role, you will take charge of site monitoring and management throughout the clinical trial process. Your extensive knowledge of GCP will be critical in fostering effective relationships with investigator sites and ensuring patient safety. You will play a pivotal role in managing timelines, compliance issues, and the overall quality of the study execution.

Key Responsibilities:
• Oversee clinical trial activities from initiation to close-out
• Act as the main contact for investigator sites




• Address adverse events and ensure proper documentation
• Facilitate training and support for site study teams
• Submit site reports and resolve open issues quickly

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

Leverage your clinical trial expertise to enhance patient outcomes while advancing your career with Parexel.
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📌 Parexel Clinical Research Associate Role (Newfoundland and Labrador)
🏢 Parexel
📍 Newfoundland and Labrador