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

EXEC · FRACTIONALfractional.quest
University of Oklahoma
◵ OKLAHOMA CITY◷ FULL-TIME
Full-time Sr. Oncology Regulatory Specialist - CTO at University of Oklahoma, Oklahoma City
Engagement
Full-timePermanent · as posted
Days / week
Not statedClarify at apply
Day rate
Not statedNot benchmarked
IR35
Not statedClarify at apply

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.

01

Full-time Sr. Oncology Regulatory Specialist - CTO — the posting in full

~/original-posting · verbatimsource: pageup

Full-timeRate not stated Not confirmed still open

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.

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