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Research Coordinator II, Administrative Research, Full Time, Days
Prisma HealthGreenville, SC
Posted Oct 13, 2026
What you’d do
Coordinates day-to-day management of clinical trial research studies, including data collection and submission, protocol compliance, participant visits and safety monitoring. Full time, days. Found on the employer's careers page on Oct 17, 2026. Apply through the link.
You’ll need
- Bachelor's in Health Sciences or Business-related field
- 2 years research experience (pharma, academic, device, NIH, investigator-initiated or registry trial
- Clinical trial protocol compliance
- Clinical data collection and submission
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