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Clinical Subjects Coordinator
A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.Provide data management and study coordination for clinical research trials.Collect quality data in timely fashion recording data on case report forms and entering into database.Work closely with staff and biostatistical core to ensure compliance and assist in the analysis of data.Register patients to trial in Clinical Trials Database/with Sponsor after confirmation of eligibility.Abstract data on patients from various sources.Participate/Organize Site Visits (UofM).


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