How do they match: Clinical Research Coordinators

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

  • Inform patients or caregivers about study aspects and outcomes to be expected.
  • Contact outside health care providers and communicate with subjects to obtain follow-up information.
  • Develop advertising and other informational materials to be used in subject recruitment.
  • Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.
  • Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
  • Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
  • 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.
  • Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.

  • Manage operations, research, or logistics projects.
  • Manage organizational or project budgets.
  • Code data or other information.
  • Communicate organizational information to customers or other stakeholders.
  • Coordinate with external parties to exchange information.
  • Interview employees, customers, or others to collect information.