Senior Clinical Research Associate/CRA - FSP
Job Description
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.
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.
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.
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.