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Vice President, Global Program Head

Job in Wilmington, New Castle County, Delaware, 19894, USA
Listing for: Incyte
Full Time position
Listed on 2026-09-12
Job specializations:
  • Management
    Healthcare Management, Project & Program Management
Salary/Wage Range or Industry Benchmark: 250000 - 350000 USD Yearly USD 250000.00 350000.00 YEAR
Job Description & How to Apply Below

Overview

Incyte is a global, science-driven biopharmaceutical company recognized for its strong growth and deep commitment to advancing therapies in Hematology, Oncology, and Immunology. With a diverse and expanding early pipeline, Incyte is shaping the next generation of targeted and immune-based therapies. Our strength lies in our ability to combine scientific insight with clinical execution, transforming discoveries into impactful medicines for patients worldwide.

We are a company in motion, growing, evolving, and investing in early development as a core engine of innovation. At Incyte, every idea begins with science — and every scientist plays a part in shaping what comes next.

The Vice President Global Program Head (GPH) – Dermatology, Immunology is responsible for leading cross-functional teams to advance early-stage dermatology and immunology programs. This role owns the integrated product development strategy and ensures delivery of programs aligned with corporate priorities, timelines, budgets, and quality standards.

Key Responsibilities
  • Program Leadership & Strategy:
    • Lead global development strategy for assigned product(s), maximizing overall asset value.
    • Develop and deliver integrated product development plans, incorporating:
      • Clinical development strategy
      • Commercial target product profile
      • CMC/pharmaceutical development plans
    • Ensure alignment with corporate strategy and therapy area priorities.
    • Contribute to broader therapy area strategy and sub-team leadership.
  • Execution & Delivery:
    • Accountable for delivering programs on time, within budget, and to required quality standards.
    • Lead cross-functional teams through strategic planning and execution of development programs.
    • Partner with Project Management to:
      • Maintain high-quality risk management plans
      • Identify, assess, and mitigate key risks
      • Escalate significant risks based on likelihood and impact
    • Track program progress, proactively addressing issues related to timelines, budget, and resources.
    • Escalate major variances to governance bodies as appropriate.
  • Cross-Functional Collaboration:
    • Collaborate across functions (clinical, regulatory, CMC, commercial, preclinical, operations, etc.) to ensure:
      • Appropriate expertise is embedded in programs
      • High-quality decision-making and execution
    • Ensure teams are appropriately resourced and staffed with the necessary capabilities.
    • Identify and upscale resource gaps impacting delivery or quality.
  • Leadership & Team Effectiveness:
    • Lead and inspire cross-functional project teams, fostering a high-performing, collaborative environment.
    • Drive accountability, ownership, and focus on results.
    • Empower team members with clear direction aligned to organizational goals.
    • Promote a global, enterprise-first mindset.
  • Operational Excellence:
    • Proactively identify risks, challenges, and opportunities; take action to reduce cycle times.
    • Ensure decisions are made at the appropriate level with cross-functional input.
    • Maintain accurate, current, and approved program documentation.
  • Insights & External Awareness:
    • Stay current on industry trends, regulatory changes, and scientific advancements in dermatology and immunology.
    • Apply insights to active programs and contribute to R&D and therapy area strategy.
Qualifications & Experience
  • Deep expertise in translational dermatology and/or immunology.
  • Minimum of 15 years in the pharmaceutical industry, including at least 10 years in leadership roles in early development.
  • Proven track record leading lifecycle management and early-stage development programs.
  • Experience successfully delivering global regulatory submissions (e.g., NDA, BLA, MAA, JNDA).
  • Demonstrated leadership of cross-functional teams across all stages of drug development.
  • Strong knowledge of drug development processes, including clinical (Phase I–III), CMC, and preclinical.
  • Excellent communication and presentation skills, including experience presenting to senior executive leadership.
  • Willingness and ability to travel domestically and internationally as needed.
Core Competencies
  • Collaboration & Teamwork:
    Builds strong partnerships across functions; prioritizes enterprise goals; fosters inclusive, high-performing teams.
  • Results Orientation:
    Drives accountability and delivers outcomes that meet or exceed expectations; maintains a strong customer focus.
  • Leadership:
    Inspires, develops, and empowers individuals and teams to achieve strategic goals.
  • Functional Expertise:
    Demonstrates deep knowledge of end-to-end drug development and regulatory processes.

Disclaimer:
The above statements are…

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