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Sentara Health is hiring a Clinical Research Coordinator for the Clinical Trials office. This is a TEMPORARY Full-time, Day shift position. Working hours are 8:00 am to 4:30 pm. Local travel throughout Hampton Roads is required on a daily basis. The project is estimated to continue for approximately 12 months. Temporary assignments do NOT offer benefits. Manages and coordinates all aspects of conducting clinical trials within Sentara Health, both clinically and administratively. Utilizes in-depth knowledge of protocol requirements to ensure that studies are properly conducted in conformance with the protocol guidelines, departmental standards and good clinical practices as set forth by federal regulations. Sound conduct of the clinical trial including recruitment, screening, enrollment and follow-up of eligible subjects according to protocol requirements. Maintenance of accurate and complete documentation of related regulatory documents. As the primary resource for the protocols, will act as liaison between the investigators, the institutional review board (IRB), and the sponsor.