Clinical Research Coordinator

Purpose (Objective): The Clinical Research Coordinator is an essential team member in the conduct of dietary, exercise and pharmaceutical studies. This position acts as a point person for the clinical-study site, overseeing all operational responsibilities for the successful launch, enrollment, maintenance and completion of clinical projects. This position will report to the Clinical Site Manager. Main activities: ● Recruit, screen and enroll clinical study participants. ● Obtain proper written informed consent from each study participant prior to participation in the study. ● Schedule and complete defined activities of the studies completely and accurately. ● Develop source documents and tools specific to the protocol. ● Accurately complete source documents/case report forms, study medication and product accountability. ● Train and brief current and new staff on all operational policies and procedures of the study, ensuring each person understands his/her role and responsibilities in the study. Ensure that the clinical trial is conducted according to the investigational plan (protocol) and Good Clinical Practices. ● Meet and communicate with the Sponsor and/or their designee regarding the conduct of the study. ● Inform Institutional Review Board and Sponsor as appropriate of relevant adverse events. ● Successfully interact with the clinical research team. ● Maintain a high level of knowledge and understanding of assigned protocols. ● Support the corporate quality and continuous improvement process (TQM). ● Perform other duties as needed. Communication: Internal Interlocutors: Internal Clinic Operations External Interlocutors: Clients