Senior Clinical Research Associate/CRA - FSP

<div> <div data-turn-id-container="request-WEB:4e8fd62a-3653-4489-a50c-fa50a74f4119-22" data-is-intersecting="true"> <section data-turn-id="request-WEB:4e8fd62a-3653-4489-a50c-fa50a74f4119-22" data-turn-id-container="request-WEB:4e8fd62a-3653-4489-a50c-fa50a74f4119-22" data-testid="conversation-turn-14" data-scroll-anchor="false" data-turn="assistant" dir="auto"> <div> <div data-conversation-screenshot-content=""> <div> <div data-message-author-role="assistant" data-message-id="2b699fa2-8bd4-4c25-9dcf-41bf7300a530" data-message-model-slug="gpt-5-3-mini" data-turn-start-message="true" tabindex="0" dir="auto"> <div> <div> <p data-start="0" data-end="193"><strong>This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Clinical Research Associate (CRA) - FSP based in Canada.</strong></p> <p data-start="195" data-end="1211">This is a field-based clinical operations role focused on ensuring the successful execution of clinical trials through high-quality site monitoring, patient safety oversight, and strong investigator site relationships. You will act as the primary point of contact for assigned study sites, supporting them from activation through close-out while ensuring compliance with ICH-GCP, local regulations, and sponsor requirements. The role requires a strong balance of scientific understanding, operational discipline, and relationship management to drive site performance, enrollment success, and data quality. You will work closely with cross-functional study teams, including site care partners and clinical operations stakeholders, to resolve issues and maintain trial timelines. With a strong focus on oncology and other complex therapeutic areas, this role plays a key part in safeguarding patient safety and ensuring high-quality clinical data. This is a remote position within Canada requiring up to 60–80% travel.</p> </div> </div> </div> </div> </div> </div> </section> </div> </div>