Advance your career as a Senior Clinical Research Associate specializing in cardiovascular studies across Canada's West region. This unique role offers a blend of on-site and remote site management responsibilities.
As a Senior CRA, you will assess site processes, conduct interim monitoring, and manage site compliance with regulatory guidelines. Successful candidates will demonstrate excellent communication skills, critical thinking, and the ability to oversee complex clinical trials while managing significant travel for site visits.
Key Responsibilities: • Execute site qualification, initiation, and close-out visits • Verify documentation of informed consent and monitor patient confidentiality • Conduct detailed reviews of site medical records and documents • Ensure proper handling of investigational product inventory • Track project activities and maintain up-to-date communications logs