IIT Research Program Coordinator
About The Position
OU Health Stephenson Cancer Center is Oklahoma’s only National Cancer Institute (NCI)-Designated Cancer Center, and one of only 73 NCI-Designated Cancer Centers in the United States. This highly competitive accreditation ensures that our patients receive the highest standard of care and have access to the most advanced cancer treatment options. At the Stephenson Cancer Center, we have an exciting new job opportunity that could be right for you! Where clinical research innovation meets real world impact: Are you energized by complex projects, collaborative science, and the opportunity to directly advance patient centered research? Do you thrive at the intersection of coordination, compliance, and discovery? Join our Investigator Initiated Trials (IIT) Program and play a critical role in transforming bold research ideas into active, compliant, and impactful clinical trials. We’re seeking an IIT Research Program Coordinator who is passionate about clinical research, detail oriented in execution, and confident leading studies from concept through activation and beyond. As an IIT Research Program Coordinator, you’ll work side by side with investigators, clinicians, regulatory teams, and external collaborators across the state and nation. Your work will support cutting edge, investigator driven clinical trials—often from the first idea all the way through data analysis and regulatory submission. Every day is different. Every study matters. This is more than a coordination role—it’s a chance to be a driving force behind investigator led clinical discovery. If you’re ready to grow your career in clinical research while supporting meaningful, high impact trials, we’d love to have you on our team.
Requirements
- Bachelor's degree in Nursing or Health Professions field.
- 24 months experience in nursing, healthcare, or clinical trials management.
- Current State licensure if the department requires an RN or Physician Assistant.
Responsibilities
- Play a critical role in transforming bold research ideas into active, compliant, and impactful clinical trials.
- Support cutting edge, investigator driven clinical trials—often from the first idea all the way through data analysis and regulatory submission.
- Work side by side with investigators, clinicians, regulatory teams, and external collaborators across the state and nation.
Benefits
- Benefits Eligible: Yes
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
