SyndicatedFractional ExecutiveOklahoma City, Oklahoma, United States
Full-time Sr. Oncology Regulatory Specialist - CTO, University of Oklahoma
FULL-TIME EXEC JOB · OKLAHOMA CITY, OKLAHOMA, UNITED STATES

Full-time Sr. Oncology Regulatory Specialist - CTO at University of Oklahoma, based in Oklahoma City. Full posting below, with the day rate stated or estimated with its basis.
Full-time Sr. Oncology Regulatory Specialist - CTO — the posting in full
~/original-posting · verbatimsource: pageup
Pay Range: Targeted pay range of $18.60 - $24.18 hourly, based on experience.
Benefits Eligible: Yes
Work Schedule: Monday – Friday, Standard/Fixed Schedule
Travel: Not required
- Position Introduction:
- OU Health Stephenson Cancer Center is Oklahoma’s only National Cancer Institute
- (NCI)-Designated Cancer Center, and one of only 74 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.
Senior Oncology Regulatory Specialist – Clinical Trials Office
- At the Stephenson Cancer Center, we’re accelerating the future of cancer care
through research that changes lives. As part of our mission to advance
world‑class oncology science, we’re excited to offer a high‑impact opportunity
for a skilled Senior Oncology Regulatory Specialist to join our Clinical Trials
Office.
In this role, you’ll serve as a regulatory expert—operating with independence,
expertise, and sound judgment. You’ll coordinate essential IRB submissions,
manage informed consent revisions, support grant activities, and ensure every
study aligns with the highest standards of ethics, compliance, and scientific
rigor. Your work will directly support the clinical research teams driving
breakthroughs in oncology.
Learn more about the Stephenson Cancer Center’s Clinical Trials Office.
[https://www.ouhealth.com/stephenson-cancer-center/cancer-research/cancer-shared-resources-services/clinical-trials-office/]
What You’ll Do
- Track and manage regulatory submissions for oncology clinical trials.
- Manage informed consent updates to ensure clarity and compliance.
- Support Cancer Center Strategic initiatives and NCI reporting requirements
- with regulatory documentation.
- Ensure adherence to University Compliance, Code of Ethics, and Business
- Standards.
- Guide study teams through regulatory requirements.
- Maintain audit‑ready records and essential documents.
- Collaborate across departments to streamline regulatory workflows.
- This is your chance to join a nationally recognized cancer center where your
- regulatory expertise fuels discoveries, protects patients, and drives meaningful
- progress in oncology research.
View full job description
[https://apps.hr.ou.edu/JobDescription/Home/Details/7438]
Required Education and Experience:
- Bachelor's Degree.
- Equivalency/Substitution: Experience or a combination of education & related
experience can be considered in lieu of degree. A one-to-one ratio is used to
determine the number of years of experience required in place of a degree.
Same role · same category
Similar Fractional Executive jobs
More on the board
Other live fractional & interim jobs
Latest on the board
Featured fractional roles
Explore the category
Browse every fractional leadership role
not quite the right fit?
Tell us what you're actually looking for.
Browse the UK fractional and interim roles on our board — each day rate stated, estimated with its basis, or marked not stated — flagged when a role is worth a fractional pitch.
Hiring for a role like this? We undertake a shortlist of 3–5, five-stage vetting and an IR35 position on every brief.