Responsible for oversight of assigned clinical research projects to ensure high quality data is obtained to support regulatory and marketing needs. This position takes a support or lead role in site initiation and interim monitoring, periodic reporting of study results, and other related activities. The documentation maintained by this position is critical in supporting successful inspections/audits of Exactech’s clinical studies. If you are an experienced clinical study coordinator looking to become a CRA/Monitor - check out this opportunity. The position involves traveling to include both remote & onsite monitoring. Duties & Responsibilities (Key Deliverables): Monitor the progress of clinical studies at investigative sites and ensure tha
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