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Under limited supervision, responsible for actively facilitating clinical research by administering and monitoring treatment or research protocols. Coordinates and participates in clinical research studies conducted by principal investigator; coordinates and participates in a variety of complex activities involved in the recruitment, implementation, regulatory communications of study protocols, collection, compilation, documentation and analysis of clinical research data. Assists in the determination of guidelines for the collection of clinical data and/or administration of clinical studies. May lead or mentor lower level team members.
Date Posted: 22 October 2024
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