Onsite Clinical Trials Data Entry Specialist - St. Louis
Medix™
Medix™ is hiring a Data Entry Coordinator for onsite work in St. Louis, MO. In this full-time role, you will support clinical trials by entering and reviewing study data in research databases and ensuring HIPAA/GCP compliance. The ideal candidate has 1+ year of clinical research experience and familiarity with EDC systems, data quality checks, and research documentation. Ophthalmology research is a plus but not required. #J-18808-Ljbffr Medix™
Vacancy posted 5 days ago
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