Clinical Research Coordinator

University of Oklahoma•Oklahoma City, OK
•Onsite

About The Position

Join a dedicated, fast-growing Maternal-Fetal Medicine research team and support the development, activation, and daily conduct of perinatal clinical research studies. The role works closely with maternal-fetal medicine physicians, sonographers, obstetric nurses, patients, and families to support participant safety, regulatory compliance, and research excellence. It also serves as a liaison among study participants, investigators, research sponsors, institutional review boards, and multidisciplinary clinical care teams across outpatient clinics and labor and delivery units. Research activities occur in an active, 24/7 clinical hospital setting and labor and delivery unit. Although the listed work schedule is Monday through Friday, 8:00 a.m. to 5:00 p.m., the posting also says the anticipated schedule covers late afternoon into evening hours and may include rotating weekends and holidays for clinical trial coverage and patient enrollments. Travel is not required.

Requirements

  • Bachelor's degree and 12 months of clinical practice, nursing, or clinical trial or research program coordination experience.
  • In lieu of a bachelor's degree, 48 months of equivalent experience may be accepted, for a total of 60 months of experience.
  • A master's degree may be accepted in lieu of experience.
  • Basic Life Support (BLS) certification.
  • Oklahoma State licensure is required for nurses and physician assistants.

Nice To Haves

  • Fluency in English and Spanish; Spanish fluency is strongly preferred.
  • Phlebotomy certification or demonstrated experience collecting, processing, and handling biological specimens.
  • Experience with REDCap database management, data entry, and workflow tracking.

Responsibilities

  • Support the development, activation, and daily conduct of perinatal clinical research studies.
  • Work with maternal-fetal medicine physicians, sonographers, obstetric nurses, patients, and families to support participant safety, regulatory compliance, and research excellence.
  • Serve as a liaison among study participants, investigators, research sponsors, institutional review boards, and multidisciplinary clinical care teams across outpatient clinics and labor and delivery units.
  • Support clinical trial coverage and patient enrollments, including during anticipated late afternoon and evening hours and potentially rotating weekends and holidays.

Benefits

  • Benefits eligible; specific benefits are not listed.
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