VP of Regulatory Affairs in Oncology

VP of Regulatory Affairs in Oncology About the Company A globally-recognized pharmaceutical company focusing on innovative treatments. Industry Pharmaceuticals Type Privately Held Founded 2023 Employees 1001-5000 Funding $101-$200 million Categories Pharmaceuticals Medicine Manufacturing Chemical Products About the Role We are excited to invite applications for the position of Vice President of Regulatory Affairs in Oncology. This critical leadership role requires a strategic thinker with extensive oncology experience. You will spearhead the development of comprehensive regulatory strategies for our non-clinical and clinical programs, overseeing IND and NDA submissions and fostering global regulatory interactions. Your responsibilities will include: Leading regulatory agency engagements to propel our oncology initiatives. Providing vision and operational leadership to cross-functional teams. Ensuring our promotional materials meet FDA regulations and internal policies. Holding accountability for regulatory submissions and maintaining compliance across both new and established programs. Ideal candidates will possess an advanced degree in a relevant scientific discipline, with a preference for a doctoral degree, and at least 15 years of experience in the biopharmaceutical sector—10 of which should focus on regulatory affairs in oncology. Demonstrated success in preparing and submitting regulatory applications for drug or biologic products, especially in the context of NDA submissions, is crucial. We seek a proven leader who is adept at navigating complex regulations, balancing immediate needs with a long-term vision, and driving results while fostering stakeholder collaboration. If you are dedicated to continuous improvement and innovation in a dynamic environment, we encourage you to apply. Hiring Manager Title Chief Medical Officer Travel Percent Less than 10% Functions Medical Care/Hospital Administration

Created: 2026-03-10