How do they match: Clinical Research Coordinators

  • Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
  • 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.
  • Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.

  • Maintain operational records.