The primary responsibility of the Clinical Research Coordinator is to manage all aspects of conducting clinical trials. The Research Coordinator is required to have an in-depth knowledge of protocol requirements and good clinical practices. As the primary resource for the protocols, you will act as liaison between the investigators, primary care providers, the institutional review board and the sponsor. You will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring. You will also be responsible for all data and source documentation, adverse experience reporting, and regulatory files. RN, LVN or equivalent experience, or Certification as a Clinical Research Professional plus at least 2 years experience as a study coordinator. |
