Sr. Clinical Research Nurse

University of Oklahoma

  • Oklahoma City, Oklahoma
  • 30+ days ago

    Highlights

    The Research Nurse / Clinical Research Coordinator supports the clinical research mission of the Department of Surgery by coordinating the day-to-day operations of industry-sponsored and investigator-initiated clinical trials. This person will serve as a primary point of contact for study participants, ensuring that enrollment, consent, and data collection are conducted with rigor, compassion, and regulatory precision.

    Numbers & Facts

    LocationOklahoma City, Oklahoma

    Description

    Pay Range: Targeted salary of $72,500, depending on education and experience.

    Benefits Eligible: Yes

    Work Schedule: Monday – Friday, 8:00 a.m. to 5:00 p.m.

    Travel: Not required

    For Best Consideration Date: 8/1/2026

    Position Introduction:

    The Research Nurse / Clinical Research Coordinator supports the clinical research mission of the Department of Surgery by coordinating the day-to-day operations of industry-sponsored and investigator-initiated clinical trials. This person will serve as a primary point of contact for study participants, ensuring that enrollment, consent, and data collection are conducted with rigor, compassion, and regulatory precision.

    View full job description.

    Required Education:

    • Bachelor's Degree in Nursing.
    • 48 months professional (RN) experience in a research capacity.

    Substitution/Equivalency: Will accept an Associate's Degree in Nursing and 24 months professional (RN) experience.

    Required Certifications and Licenses:

    • State of Oklahoma Registered Nurse Licensure
    • Basic Life Support (BLS) certification
    • Cardiopulmonary Resuscitation (CPR) certification

    Department Preferences:

    • Clinical assessment skills and familiarity with surgical or perioperative patient populations (if RN)
    • Experience with industry-sponsored trials and sponsor/CRO monitoring visits
    • Familiarity with electronic data capture systems (REDCap, Medidata Rave, or similar)
    • Working knowledge of iRIS or comparable electronic IRB submission system
    • Experience with study startup, including budget and contract review
    • CCRP (Certified Clinical Research Professional) or CCRC (Certified Clinical Research Coordinator) credential, or interest in pursuing
    • Bilingual (Spanish/English) skills are a plus given our patient population
    • 2 or more years of clinical research coordinator experience, ideally with both industry-sponsored and investigator-initiated studies
    • Experience in surgical, oncology, pediatric, or other procedural research settings
    • RN candidates: active clinical nursing experience in addition to research experience

    Hiring Contingent Upon a Background Check: Yes

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