Regulatory Affairs Lead - Oncology Trials; Hybrid, Denver
Listed on 2026-10-07
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Healthcare
Oncology Care
US Oncology Inc. seeks an experienced Regulatory Affairs Coordinator in Denver to manage regulatory activities for clinical trials. The role requires ensuring regulatory compliance, maintaining essential documents, and coordinating IRB submissions.
The ideal candidate has 7+ years in clinical research or oncology regulatory affairs, with experience in Phase 1-4 trials and strong communication and organizational skills. Hybrid schedule, onsite two days weekly.
We invite applications for the Regulatory Affairs Lead - Oncology Trials (Hybrid, Denver) position located in Denver, CO, United States.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Denver, CO, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Management & Operations.
The advertised compensation is 65.000 - 95.000.
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