Develops and maintains liaison with clinical investigators, medical educators, clinical research organizations (CRO), affiliated hospitals, state and/or government hospitals, and research institutions to initiate and expedite clinical studies on products that have investigational new drug or medical devices approval.
Responsible for reviewing adverse event cases with investigators, determining and monitoring time schedules, preparing study documents, and issuing status reports.
May assist with design, development, and monitoring of clinical evaluation projects.
Training investigators and site personnel including headquarter and field clinical research associates (CRA).
Contacting and recommending qualified investigators to perform studies and initiate clinical trials.
