How do they match: Clinical Research Coordinators

  • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.

  • Advise customers on technical or procedural issues.
  • Communicate organizational information to customers or other stakeholders.
  • Communicate with government agencies.
  • Interview employees, customers, or others to collect information.