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Clinical Research Coordinator (Full Time, Days)
Description Job Summary Coordinates clinical research studies on human subjects. Responsible for subject recruitment, follow-up, data management, detailed record keeping and regulatory compliance, report writing, and correspondence with investigators, IRBs, and regulatory authorities. Responsible for the new submission of protocols with subsequent amendments. Some participation in protocol writing, and initial and continuing education for Good Clinical Practice compliance. Minimum Job Requirements AA/medical/technical school or 3 year of research and/or healthcare experience required Qualifications


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