REQ-10072898
Feb 27, 2026
LOC_GB

About the Role

Major Accountabilities:

  • Lead development and execution of medical affairs strategy for TA/Asset priority programs including transformative tactics such as research/population health, innovative partnerships and integrated evidence plans
  • Co-develop plans for evidence generation, MSL / Field Medical Affairs strategy, medical education programs, scientific publication planning and Medical Expert network development with TAs
  • Co-own the development and implementation of innovative education and scientific communication plans for external stakeholders
  • Financial tracking to ensure timely and cost-effective development & execution of medical activities
  • Prepare Scientific review committee submissions for TA assets
  • Partner with Development, S&G, US and International medical affairs, cross-functions to shape portfolio early and diversify evidence to achieve broad access at launch and to enhance impact on clinical practice for priority programs
  • Represent GMA around prioritized portfolio with internal and external audiences, in collaboration with TAs including the investment, medical and regulatory communities, as well as pharmaceutical or biotechnology industry collaborators/partners
  • Represent “the voice of the patient” internally and evaluate factors relevant to a patient’s informed decision making
  • Provide direction and input into the development and implementation of successful reimbursement and market-access strategies
  • Provide proactive input to Development on potential new therapeutic indications, to enrich Registration Programs and to consider new therapeutic opportunities.
  • Ensure that Patient Access programs are supported for all brands within the GMA and delivered with full compliance
  • Ensures GMA activities are designed and executed in compliance with company policy guidelines and highest medical quality standards
  • Provide proactive medical input to asset lifecycle management to consider new therapeutic opportunities

Requirements:

Must have:

  • MD, Neurologist (Preferred) or PhD/PharmD in Neuroscience/ Health Sciences. Specialist Degree or specialist qualification in Gene therapy related to discipline for which is responsible is an advantage
  • 3+ years in Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development
  • Critical thinker and with ability to navigate uncertainty without major supervision
  • Fluent oral and written English; Other relevant languages are an advantage.
  • Strategic mindset and able to establish credibility and influence across a range of diverse stakeholders in a matrix organization to drive change
  • Ability to truly collaborate across functions and markets: serve-partner-co-create
  • Able to navigate in an environment of shared outcomes and cross-business accountabilities
  • Deep understanding of health care systems and key external stakeholders
  • Strong track record of delivery focus for time and quality in medical affairs projects
  • Successful development and implementation of innovative programs and processes
  • Understands unmet medical needs, generates the right evidence to fulfil them, uses innovative, multichannel communication formats for effective evidence dissemination
  • Credibility as peer expert with external stakeholders
  • Agile mindset & ability to lead in an agile organization across Disease Areas
  • Firm working knowledge of GCP, scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies designated for review by regulatory authorities.

Preferred

  • Highly preferred: Neuromuscular, Rare Disease, siRNA, Gene Therapy expertise, significant medical affairs early asset lifecycle, pre-launch and launch experience in Global organizations
  • Experience in developing and executing “Best in Class” processes at scale
  • Clinical trial research experience conducted in a pharmaceutical or equivalent academic environment in TA of interest is strongly desired.

Commitment to Diversity & Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.

Role Requirements

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)

DIV_GD
Marketing
LOC_GB
London (The Westworks)
LOC_IE
LOC_ES
FCT_RD
Full time
Regular
No
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REQ-10072898

Medical Director, Neuroscience, Global Medical Affairs

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