Clinical Studies Coordinator

2 weeks ago


ValdeReuil, Normandie, United States Wake Forest University School of Medicine Full time
Job Summary

Under general supervision, responsible for the compilation and collection of data, recruitment of subjects, and general coordination of clinical studies. This role requires strong organizational and communication skills, as well as the ability to work effectively in a team environment.

Key Responsibilities
  1. Assists principal investigator and other health professionals in troubleshooting various problems related to the management of the clinical study.
  2. Performs technical procedures on clinical subjects under the direction of the principal investigator or his/her designee.
  3. Assists with recruitment of patients for the clinical study, including tracking the sources of patient referrals and following up with referring doctors and other sources.
  4. Maintains appropriate patient records, including charting the condition of the patient and determining their continued eligibility in the study.
  5. Obtains and interprets pertinent data from medical records as needed to understand past and present condition of the patients.
  6. Performs day-to-day administrative and clerical duties, including designing brochures, stationery, and data forms, and creating reports and graphs pertinent to the study.
  7. May supervise other personnel, including volunteers, as assigned.
  8. Assists in development of suitable codes and data collection forms for computerization.
  9. Consults and cooperates with all faculty, coordination centers, sponsors, and health professionals involved in the clinical study.
Work Environment

Clean, well-lit, office environment and community settings.

About Us

Wake Forest University School of Medicine is a U.S. News and World Report top 50 ranked medical school, integrated with a world-class health system, Atrium Health. We are committed to improving health, elevating hope, and advancing healing - for all.



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