Responsibilities

• 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) ...