How do they match: Clinical Research Coordinators

  • Clinical Manager
  • Clinical Program Manager
  • Clinical Project Manager
  • Clinical Research Nurse
  • Clinical Research Nurse Coordinator
  • Clinical Research Manager
  • Clinical Study Manager
  • Clinical Trial Manager
  • Clinical Trials Manager

  • Register protocol patients with appropriate statistical centers as required.
  • Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
  • Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
  • Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
  • Participate in preparation and management of research budgets and monetary disbursements.
  • Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
  • Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.

  • Manage operations, research, or logistics projects.
  • Manage organizational or project budgets.
  • Conduct financial or regulatory audits.
  • Maintain regulatory or compliance documentation.
  • Monitor organizational compliance with regulations.