Clinical Research Coordinator

3 weeks ago


Austell, Georgia, United States Wellstar Health System Full time
Job Summary

The Clinical Research Coordinator will be responsible for managing clinical trials for the Clinical Trials Office of the WellStar Health System. This includes identifying potential study patients, ascertaining patient eligibility, coordinating and evaluating patients in clinical trials, and maintaining records for patients enrolled in clinical trials.

Key Responsibilities
  • Conduct all aspects of clinical trials, including consenting, using Good Clinical Practice, FDA, and Institutional guidelines.
  • Review patient charts for eligibility requirements and enroll patients according to protocol guidelines.
  • Communicate with physician/office staff regarding scheduling protocol-specific requirements.
  • Attend patient visits and gather protocol-specific information when required.
  • Coordinate the dispersement of protocol-provided drug therapy.
  • Ensure that Investigation Product chain-of-custody practices are instituted and documented.
  • Communicate effectively with Research Assistants and other research staff.
  • Submit required documentation within designated time frames.
Additional Responsibilities
  • Prepare research charts for monitoring visits and audits.
  • Follow guidelines and timelines for reporting Adverse Events and Deviations.
  • Maintain current protocols with revisions, amendments, and current IRB-approved informed consent.
  • Ensure clinical trial and sponsor-required training is completed.
Requirements
  • Graduate from an approved school of nursing.
  • Minimum 5 years RN experience required.
  • Minimum 2 years research experience.
  • Strong computer skills.
  • Good oral and written communication skills.
  • Excellent interpersonal and organization skills.


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