Clinical Trials Coordinator: Manage Study Visits & Data
Listed on 2026-10-13
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Healthcare
Clinical Research -
Research/Development
Clinical Research
Planet Pharma seeks a Clinical Research Coordinator to coordinate study visits in line with ICH-GCP and IRB-approved protocols. The role includes consent, eligibility screening, data collection, sample handling, EDC entry, and site coordination.
Ideal candidates have proven clinical trials experience, strong organizational and communication skills, and familiarity with Microsoft Office. On-site collaboration and patient-focused support are essential.
Our organisation is growing, and we are hiring a Clinical Trials Coordinator:
Manage Study Visits & Data in Pleasant Hill, OH, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the Clinical Trials Coordinator:
Manage Study Visits & Data role in the description above.
We appreciate your interest in this position.
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