Clinical Research Coordinator

1 month ago


San Marcos, United States Medix™ Full time

We are seeking a detail-oriented Clinical Research Coordinator to join our team. In this role, you will be responsible for coordinating and managing clinical research studies, ensuring compliance with protocols, and maintaining accurate documentation. You will work closely with investigators, participants, and sponsors to facilitate study activities, including participant recruitment, data collection, and reporting. The ideal candidate has excellent organizational skills, experience in clinical research, and a strong understanding of regulatory requirements.

Key Duties:

  • Coordinate and manage day-to-day activities of clinical research studies.
  • Recruit, screen, and enroll study participants according to protocol.
  • Obtain informed consent and ensure participants' rights and safety.
  • Collect, process, and manage biological samples and clinical data.
  • Maintain accurate and detailed records of study-related activities.
  • Monitor participant progress and report any adverse events.
  • Ensure compliance with Good Clinical Practice (GCP) and regulatory requirements.
  • Prepare and submit study documents to Institutional Review Boards (IRBs).
  • Assist in the development and revision of study protocols and procedures.
  • Collaborate with investigators, sponsors, and regulatory bodies to ensure smooth study conduct.



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