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We are looking for a full-time experienced clinical research study coordinator to assist in conducting phase II-IV clinical research trials. We are a dedicated team of physicians, RN’s, and administrators committed to high-quality patient care and strict adherence to GCP’s through the entire clinical trial process.
Candidates must be hard working, detail-oriented, team players who want to join our team. Must work well under pressure, be willing to meet multiple and competing deadlines, demonstrate professionalism in interactions with patients, sponsors,etc.
Duties include: Meet with patients and follow study protocol procedures, Maintain patient charts, Other duties as assigned.
Job Type: Full-time
Benefits:
Work Location: In person
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