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Clinical Research Coord Inter
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.The successful candidate will be responsible from helping to identify potential study participants, keep in contact with them, helping to create schedules for the study participants, obtaining informed consent after being trained, keeping study documents, submitting documents to the regulatory bodies after appropriate training and oversight, preparing data reports, assisting to create and maintain study databases together with other study
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