How do they match: Clinical Research Coordinators

  • Organize space for study equipment and supplies.
  • 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.
  • Solicit industry-sponsored trials through contacts and professional organizations.

  • Communicate organizational information to customers or other stakeholders.
  • Confer with organizational members to accomplish work activities.
  • Develop organizational methods or procedures.
  • Manage organizational or project budgets.
  • Monitor organizational compliance with regulations.