Wednesday, May 19, 2010

Clinical Research Position Available

Full time position will manage all aspects of clinical research studies. Responsibilities will include obtaining patient consents, assuring adequate protection of subjects, ensuring compliance with protocol guidelines and requirements of regulatory agencies, ensuring the accuracy and quality of patient data collected and study documentation. Must possess excellent interpersonal, communication and organizational skills. Two years experience as a site level study coordinator and phlebotomy skills required. Clinical Research Coordinator certification preferred.

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