The Profile Created position at Medpace involves assisting with the coordination and management of clinical trials. Responsibilities include data entry, documentation review, and communication with study participants. The ideal candidate will have a Bachelor's degree in a related field, at least two years of experience in clinical research, strong attention to detail, and excellent communication skills. Proficiency in Microsoft Office suite and knowledge of GCP guidelines are also required. This is an entry-level position suitable for candidates looking to start their career in the healthcare or pharmaceutical industry.
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