Clinical Trials Specialist: GCP, Site Management & Study Design

Greenkey Resources LLC is looking for a Clinical Research Specialist in Minneapolis, Minnesota. The ideal candidate will design and oversee clinical evaluation studies, ensuring compliance with Good Clinical Practice (GCP). Responsibilities include preparing study documentation, managing trial operations, and providing mentorship to junior staff. Candidates must have a Bachelor's degree and at least 2 years of relevant experience. Strong communication and project management skills are essential for success in this collaborative role.
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