Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Sr. Clinical Research Nurse

Job

University of Oklahoma

Norman, OK (In Person)

$72,500 Salary, Full-Time

Posted 1 week ago (Updated 3 days ago) • Actively hiring

Expires 8/2/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
65
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job 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