Executive Director, Portfolio & Pipeline Strategy

Novartis AGEast Hanover, NJ
76d$214,900 - $399,100Hybrid

About The Position

The Executive Director, Portfolio and Early Pipeline Strategy is responsible for leading a team that is cross-functionally accountable for building the foundation for sustainable and profitable growth of the TA over the 10+ year horizon. Fundamental areas of the job include building forward looking competitive readiness plans, providing input on assets to S&G, GDD and BioMedical Research, partnering with US BD&L and US Market Access, supporting strategic evaluations and initiatives, and leading Early Asset Teams to transition assets from S&G to US Commercial.

Requirements

  • Minimum 10 years of commercial experience with multiple functional experience in a pharmaceutical, biotech, healthcare, or consulting environment.
  • Recent US Market experience with launch and various product lifecycle stages.
  • Experience partnering with Medical Affairs and Global Drug Development to inform strategic choices.
  • Highly motivated individual who can work with a high degree of autonomy, in a dynamic environment applying creative problem-solving skills and industry knowledge.
  • Possess a portfolio approach and experience uncovering and implementing innovative strategies in a competitive marketplace.
  • Ability to be a leader and proactive custodian for consistent competitive readiness excellence.

Responsibilities

  • Perform strategic assessments of select competitor activities, including market situation analysis, strategic forecasting, strategic and operational benchmarking, articulation of implications and drive development of a cross-functional competitive response plan in legal and compliant manner.
  • Monitor/benchmark strategic plans and key developments of competitors to provide early warning for potential threats and opportunities for successful implementation of prioritized critical initiatives and tactical plans.
  • Proactive surveillance of core Disease Area healthcare & macroeconomic environment including policy, regulatory, health technology to identify threats and opportunities relevant to planning initiatives in the US.
  • Drive the design and execution of competitive planning initiatives (competitive simulations) for key products subject to significant competitive events.
  • Lead strategic planning for lifecycle management (LCM) across the Therapeutic Area portfolio with focus on maximizing the long-term value of our assets.
  • Work closely with cross-functional teams including Medical Affairs, Global Drug Development, Strategy & Growth, Novartis Technical Operations, Regulatory, Finance, Supply Chain, Trade and Market Access to ensure realization of LCM priorities.
  • Liaison with key cross-functional partners such as Market Access, Medical, BD&L, M&A, Biomedical Research, GDD and S&G teams to develop US go/no-go position on potential asset/company acquisition targets.
  • Inform commercial implications to early asset development plans (pre-IDPA), as well as drive development of US-centric commercialization strategy for assets in later stages (pre-FDP).
  • Develop center of excellence capabilities within the team.

Benefits

  • 401(k) eligibility
  • various paid time off benefits, such as vacation, sick time, and parental leave
  • sign-on bonus
  • restricted stock units
  • discretionary awards

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What This Job Offers

Job Type

Full-time

Career Level

Senior

Industry

Chemical Manufacturing

Education Level

Bachelor's degree

Number of Employees

5,001-10,000 employees

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