Clinical Research Coordinator

Clinical Research Coordinator

This Ideal candidate should:

  • Have at least a years’ experience as a Clinical Research Coordinator, preferably with practice coordinating industry sponsored trials in a private setting.
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Have ACRP certification, which is a plus.

Responsibilities and Duties:

  • Completing DMCR-required training, including GCP and IATA.
  • Overseeing the smooth running of clinical trials.
  • Collecting, coding and analyzing data obtained from research.
  • Managing research budgets.
  • Informing participants about study objectives.
  • Administering questionnaires.
  • Monitoring research participants to ensure adherence to study rules.
  • Adhering to research regulatory standards.
  • Adhering to ethical standards.
  • Maintaining detailed records of studies as per FDA guidelines, including things such as drug dispensation.
  • Liaising with laboratories regarding findings.
  • Participating in subject recruitment efforts.
  • Ensuring that the necessary supplies and equipment for a study are in stock and in working order.
  • Engaging with subjects and understanding their concerns.
  • Any other matters as assigned by management.