Director, Clinical Trial Portfolio Management

Role: Senior program and portfolio management leader within the PMO at CG Oncology, overseeing the development and maintenance of integrated clinical program portfolios for bladder cancer therapeutics. Responsibilities: develop strategic plans aligning clinical, regulatory, CMC, safety, and commercial workstreams; translate strategy into actionable cross-functional execution plans; lead matrixed teams to ensure milestone achievement; support risk management, governance, and inspection readiness; manage budgets, resources, and stakeholder communication. Requirements: Bachelor's in life sciences or related field; 10-15+ years in biotech/pharma with extensive experience in clinical development and program management, supporting registrational and late-phase programs; strong understanding of global regulatory pathways, GxP, and clinical trial deliverables. Preferred: demonstrated success in managing complex multi-year clinical portfolios, familiarity with bladder cancer development, and experience supporting global submissions. High-value specifics: focus on registrational and lifecycle clinical programs, cross-functional leadership across clinical, regulatory, biometrics, CMC, quality, and medical affairs; support for regulatory submissions and health authority interactions; ability to translate strategy into operational plans for biologics or immunotherapies. Work setup: Fully remote with flexible time off; domestic US work authorization required.