Advance your career in clinical research with a remote Senior Clinical Research Associate role focused on oncology. This position offers the chance to manage and monitor clinical trials across Canada.
As a Senior Clinical Research Associate, you will be accountable for all aspects of site management to uphold safety and quality in clinical trials. Your role includes monitoring investigator sites, resolving protocol-related issues, and enhancing site relationships to ensure effective enrollment and compliance. Collaborating with the Site Care Partner, you’ll contribute to the success of trials through your oncology expertise.
Key Responsibilities:
• Oversee site activities from activation to database lock
• Act as the primary contact for investigators during trials




• Perform both onsite and remote monitoring as needed
• Document and report adherence to protocols
• Address and resolve investigator site issues promptly
Requirements:
• Minimum 3 years monitoring experience required
• Oncology, vaccine, or internal medicine experience preferred
• Bachelor’s degree in life sciences essential
• Fluent in English; frequent travel (60-80%) required
• Valid driver’s license and passport mandatory
Leverage your monitoring skills and oncology background to ensure patient safety and adherence in clinical trials.
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📌 Senior CRA Oncology Focus Remote Position (Quebec City)
🏢 Parexel
📍 Quebec City