Senior Oncology Regulatory Specialist - CTO
About The Position
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. The Senior Oncology Regulatory Specialist – Clinical Trials Office role is a high impact opportunity for a skilled individual 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.
Requirements
- Bachelor's Degree.
- 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.
Responsibilities
- 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.
Benefits
- Benefits Eligible: Yes
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What This Job Offers
Job Type
Full-time
Career Level
Senior
