How do they match: Clinical Research Coordinators

  • Clinical Research Coordinators

  • Clinical Coordinator
  • Clinical Data Coordinator
  • Clinical Operations Specialist
  • Clinical Program Coordinator
  • Clinical Research Specialist
  • Clinical Research Coordinator
  • Clinical Research Nurse Coordinator
  • Clinical Support Specialist
  • Clinical Trial Coordinator
  • Clinical Trials Specialist
  • Oncology Clinical Research Coordinator
  • Program Coordinator
  • Research Coordinator

  • Plan, direct, or coordinate clinical research projects. Direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. May evaluate and analyze clinical data.

  • Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
  • Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.
  • Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
  • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.

  • Coordinate operational activities with external stakeholders.
  • Coordinate with external parties to exchange information.