Function as part of an interdisciplinary, patient‑focused team of professionals to ensure smooth and efficient facilitation of clinical trial activities
Manage day‑to‑day activities of a clinical trial including screening and recruiting eligible participants, obtaining informed consent, collecting and managing study data and ensuring compliance with protocols and regulatory guidelines
Initiate, manage, and coordinate submissions to Research Ethics Board and contracts for legal review
Communicate with internal hospital departments to complete impact assessments, facilitate departmental research agreements and obtain institutional approvals
Perform financial duties related to clinical trial activities including budget development, invoicing and study‑related patient reimbursements
Establish, maintain and complete all essential documents in the Investigator Site File (ISF) ...