Clinical Research Coordinator 240143 Job at Medix™, Wake Forest, NC

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  • Medix™
  • Wake Forest, NC

Job Description

Key Responsibilities:

  • Coordinate and oversee the day-to-day operations of clinical trials.
  • Recruit, screen, and enroll study participants.
  • Obtain informed consent from study subjects.
  • Maintain accurate and complete study documentation and records.
  • Schedule and conduct study visits and follow-ups.
  • Ensure compliance with study protocols, GCP, and regulatory guidelines.
  • Collect, process, and ship biological samples as needed.
  • Report adverse events and assist with IRB submissions.
  • Communicate with sponsors, monitors, and regulatory agencies as required.
  • Responsible for preparing and dispensing the investigational product (IP) according to randomization.
  • Maintains blinding for other staff.

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