Clinical Research Coordinator Job at Medix™, Cary, NC

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  • Medix™
  • Cary, NC

Job Description

The Clinical Research Coordinator (CRC) is responsible for coordinating and managing clinical research studies under the supervision of a Principal Investigator (PI). This role ensures that studies are conducted according to the study protocol, regulatory requirements, and institutional policies while maintaining participant safety and data integrity.

Key Responsibilities

  • Coordinate all aspects of assigned clinical trials, including participant recruitment, screening, enrollment, and follow-up.
  • Obtain informed consent from study participants.
  • Collect, record, and maintain accurate study data and documentation.
  • Schedule and conduct study visits and procedures according to protocol.
  • Communicate with sponsors, monitors, and regulatory bodies as needed.
  • Prepare and submit regulatory documents, including IRB submissions and study updates.
  • Maintain inventory of study supplies and manage investigational products (if applicable).
  • Ensure compliance with Good Clinical Practice (GCP) and institutional standards.

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