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Clinical Research Associate
Clinical Research Associate Tracking Code 350 Job Description Assists in the design, planning and conduct clinical research trials by effectively coordinating the activities of study coordinators and investigators and by ensuring compliance with study protocols, US and/or EU regulations, IRB/EC requirements and overall clinical objectives. Required Skills Two to five years related experience in coordinating multi-center clinical trials. Cardiac, critical care, ED or neuro background is preferred. Monitoring experience required. Working knowledge of FDA/EU regulatory requirements. Working knowledge of clinical trial site budget, contracts and payments. Requires travel up to 75%. Required Experience BS preferred in Life Sciences, Medicine, or other discipline or appropriate industrial...
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