Senior Oncology Regulatory Specialist - CTO

Senior Oncology Regulatory Specialist

• CTO University of Oklahoma
• 4.1 Oklahoma City, OK Job Details $38,700
• $50,300 a year 11 hours ago Qualifications Informed consent Bachelor's degree Informed consent procedures implementation Research administration Regulatory submission editing and review Communication with regulatory authorities for clinical trials Clinical research inspection readiness Senior level Ethical review application preparation Audit support Research compliance quality assurance records management Full Job Description Job no: 493108 Work type:

Technical Location:

Oklahoma City Categories:

Technology/Research Pay Range:

Targeted annual salary ranges from $38,700 to $50,300, 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 here. 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. Learn more about the Stephenson Cancer Center's Clinical Trials Office here.

Required Education:

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.

Required Certifications and Licenses:

None Hiring Contingent Upon a

Background Check:

Yes Advertised:

05 Jun 2026 Central Daylight Time Applications close: 04 Sep 2026 Central Daylight Time