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Medix™

Clinical Research Coordinator 247616

Medix™, Greenville, North Carolina, United States, 27834

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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.

Seniority Level Not Applicable

Employment Type Full-time

Job Function Research

Industries Research Services

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