REQ-10078696
May 27, 2026
LOC_CH

About the Role

Key Responsibilities

  • Define and implement integrated platform and program strategies from discovery through registration
  • Support data-driven decision-making and differentiated development strategies for the neuroscience portfolio.
  • Oversee pharmacokinetic, pharmacology, and nonclinical safety contributions to regulatory submissions and supporting documentation
  • Support health authority interactions by ensuring high-quality scientific input into development and regulatory strategies
  • Drive cross-functional collaboration across discovery, development, regulatory, and other key partner functions to ensure rigorous and efficient program execution
  • Build, lead, mentor, and develop a high-performing scientific team, including oversight of scientists based at the Basel, Cambridge, and San Diego sites.
  • Serve as a scientific thought leader internally and externally through collaborations, publications, presentations, and participation in relevant scientific forums
  • Promote operational excellence through disciplined execution, continuous improvement, and effective use of resources
  • Leverage digital tools, AI, and automation, where appropriate, to enhance insight generation, efficiency, and decision-making

Essential Requirements

  • PhD or PharmD in pharmacokinetics, pharmacology, toxicology, biomarker sciences, pharmaceutics, biochemistry, or a related scientific discipline
  • Significant biopharmaceutical industry experience, typically 12 or more years, spanning preclinical and clinical drug discovery and development, including senior leadership responsibility
  • Demonstrated people leadership experience, including hiring, mentoring, coaching, and developing scientific talent
  • Strong understanding of global regulatory requirements and experience contributing to submissions such as INDs, IMPDs, NDAs, and BLAs
  • Proven ability to work effectively in a matrixed, cross-functional environment and influence across teams and organizational levels
  • Excellent communication, strategic thinking, and problem-solving skills, with a high degree of scientific rigor and sound judgment

Desirable Requirements

  • Experience in neuroscience disease
  • Experience in bioanalytical assay development and biomarker strategy
  • Familiarity with late-stage development and registration-enabling activities
  • Experience applying digital tools, AI, or machine learning to scientific decision-making and development execution
  • Track record of external scientific visibility through publications, presentations, or industry engagement

Accessibility and accommodation:
Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message

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_RE
Research
LOC_CH
Basel (City)
FCT_RD
Full time
Regular
No
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REQ-10078696

Therapeutic Area Head, PK Science- Neuroscience

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