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Clinical Research Coordinator
Job in
Greenville, Pitt County, North Carolina, 27834, USA
Listed on 2026-01-12
Listing for:
Medix™
Full Time
position Listed on 2026-01-12
Job specializations:
-
Healthcare
Clinical Research, Medical Science -
Research/Development
Clinical Research, Research Scientist, Medical Science
Job Description & How to Apply Below
Responsibilities
- Participant Management:
Screens potential participants, explains study details, obtains informed consent, schedules visits, and acts as a primary contact for subjects. - Administrative Oversight:
Organizes study files, prepares and submits regulatory documents (like IRB submissions), manages study budgets, and maintains trial‑specific logs. - Protocol Adherence:
Ensures the trial follows the specific scientific protocol, protecting data integrity and participant safety. - Data & Documentation:
Collects, organizes, and manages research data, including case reports and drug accountability records, often working with data management teams. - Staff & Resource Coordination:
Trains research staff, arranges study equipment, and communicates with laboratories and investigators. - Ethical Compliance:
Upholds ethical standards, ensuring patient rights and well‑being are prioritized throughout the study.
Not Applicable
Employment TypeFull-time
Job FunctionResearch
IndustriesResearch Services
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