How do they match: Clinical Research Coordinators

  • Confer with health care professionals to determine the best recruitment practices for studies.
  • 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.
  • Solicit industry-sponsored trials through contacts and professional organizations.

  • Communicate with government agencies.