<ul><li>Liaise with the ethics committee regarding the rights, safety, and well-being of trial subjects.</li><li>Ordering, tracking, and managing IP and trial materials.</li><li>Overseeing and documenting IP dispensing inventory, and reconciliation.</li><li>Protecting subjects’ confidentiality, updating their information, and verifying IP have been dispensed and administered according to protocol.</li><li>Conducting regular site visits, coordinating project meetings, and writing visit reports.</li><li>Implementing action plans for sites not meeting expectations.</li><li>Liaising with regulatory authorities.</li></ul>

Clinical Research