Strategic Director, Clinical Trial Portfolio

CG Oncology, Inc.

United States

Sur place

USD 180 000 - 240 000

Plein temps

Il y a 13 jours
Générateur de candidature

Une candidature conçue pour ce poste — un CV et une lettre de motivation personnalisés qui correspondent à l’offre.

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Avantages offerts par ce poste

Fully remote
Annual bonus
Equity
401K match
Well-being benefits

Résumé du poste

CG Oncology, Inc. is seeking a Director, Clinical Trial Portfolio Management to lead the integrated portfolio across registrational and lifecycle programs, partnering with Clinical Operations, Regulatory, Medical Writing, CMC, and Commercial.

You will translate strategy into cross-functional plans, manage milestones, dependencies, risks, and governance, and drive submission readiness and readiness for global expansion.

Qualifications

  • Bachelor’s degree in life sciences, biology, engineering, or a related scientific discipline required; equivalent relevant experience may be considered
  • 10–15+ years of progressive experience in pharmaceutical/biotech, with clinical development and portfolio management experience
  • Working understanding of regulatory pathways, IND/BLA/NDA/MAA submission planning and GCP expectations

Responsabilités

  • Develop and maintain integrated development plans across registrational and lifecycle clinical programs
  • Define cross-functional timelines, milestones, dependencies, risks, and governance
  • Lead matrixed teams across Clinical Development, Regulatory, Medical Writing, Safety/PV, CMC, Biometrics, Data Management, Quality, Medical Affairs, and Commercial
  • Manage submission readiness roadmap and governance materials
  • Maintain living program risk registers and contingency plans across regulatory, safety, budget, and quality dimensions

Connaissances

Portfolio management
Cross-functional leadership
Strategic planning
Risk management
Budgeting

Formation

Bachelor’s degree in life sciences or related field

Description du poste

CG Oncology, Inc. is seeking a Director, Clinical Trial Portfolio Management to lead the integrated portfolio across registrational and lifecycle programs, partnering with Clinical Operations, Regulatory, Medical Writing, CMC, and Commercial.

You will translate strategy into cross-functional plans, manage milestones, dependencies, risks, and governance, and drive submission readiness and readiness for global expansion.

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