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Director, R&D Legal, Americas

Novartis

Cambridge, MA; East Hanover, NJHybridPosted 54 days ago$194,600 - $361,400/year
Full TimeDirector & AboveCorporate FunctionsPharmaceutical
Original posting ↗

Summary

The Director, R&D Legal, Americas will be responsible for providing strategic legal support for Research & Development activities across the Americas, including Research and Early Development, Clinical Operations, and Development Units to advance the organization's innovative pipeline.

Job description

Job Description Summary

The Director, R&D Legal, Americas will be responsible for providing strategic legal support for Research & Development activities across the Americas, including Research and Early Development, Clinical Operations, and Development Units to advance the organization's innovative pipeline.

Key responsibilities

  • Provide sophisticated legal counsel on a broad range of issues arising from R&D activities in the Americas and primarily in the U.S., including FDA regulatory requirements and development strategies, human subject protection, GxP compliance, research governance, data use and sharing, AI-enabled research, and other legal and regulatory issues impacting research and development of innovative medicines.
  • Support integration of acquired assets and programs by providing strategic regulatory and R&D legal guidance on development programs, regulatory obligations, quality systems, and operational transition matters.
  • Support the Head of R&D Legal, Americas in identifying and assessing emerging legal, regulatory, technology, and geopolitical developments impacting global R&D activities and strategic business objectives.
  • Support legal strategies and risk mitigation measures related to evolving business models, including cross-border data exchange, technology transfers, integration of acquired assets and capabilities, collaborations, and research activities involving strategically significant jurisdictions.
  • Provide legal support for clinical development and study operation activities in the Americas as needed for key initiatives, priority matters and business continuity coverage. Areas of legal support include research privacy and informed consent, site selection, patient recruitment and retention, institutional review board negotiations and approval, decentralized trials, study fees and fair market value, data use and sharing, and scientific and data integrity.
  • Provide legal support for U.S. Biomedical Research (BR) as needed for key initiatives, priority matters and business continuity coverage.
  • Partner with key stakeholders across Security & Legal, R&D, quality and regulatory to advise on the legal implications of the use of AI.
  • Support the responsible and ethical adoption of AI within R&D activities and help advance the transformation of legal service delivery through AI-enabled solutions, processes, and ways of working.
  • Legal review and advice on Novartis policies, governance frameworks, operating procedures, and training materials to ensure compliance with legal and regulatory requirements and promote effective risk management.

Essential requirements

  • Juris Doctor (J.D.) or equivalent law degree and admission to practice law in at least one U.S. jurisdiction.
  • 8+ years' post bar admission legal experience in life sciences industry (preferably biotechnology or pharmaceutical) or a top-tier law firm representing pharmaceutical clients and advising senior leaders on complex legal, regulatory, and business risks.
  • Significant knowledge of FDA law and regulation, including drug research and development, regulatory strategy, clinical development, approval pathways, GxP compliance, inspection readiness and enforcement matters.
  • Significant experience supporting development, clinical operations, quality, or related R&D organizations within a pharmaceutical or biotechnology environment.
  • Strong strategic and analytical skills, with the ability to assess novel legal, regulatory, and business issues in rapidly evolving environments.
  • Demonstrated sound judgment and ability to provide practical, risk-based legal advice on complex and ambiguous issues.
  • Demonstrated ability to learn new subject matter quickly and translate complex legal concepts into practical business advice.
  • Intellectual curiosity and interest in emerging technologies, AI, evolving regulatory frameworks, geopolitical and external factors shaping the future of pharmaceutical research and development.
  • Ability to operate effectively in an increasingly global and interconnected environment involving cross-functional, cross-border, and multidisciplinary teams.

Requirements

  • Juris Doctor (J.D.) or equivalent law degree
  • Admission to practice law in at least one U.S. jurisdiction
  • 8+ years' post bar admission legal experience in life sciences industry or top-tier law firm representing pharmaceutical clients
  • Significant knowledge of FDA law and regulation, including drug research and development, regulatory strategy, clinical development, approval pathways, GxP compliance, inspection readiness and enforcement matters
  • Significant experience supporting development, clinical operations, quality, or related R&D organizations within a pharmaceutical or biotechnology environment
  • Strong strategic and analytical skills
  • Demonstrated sound judgment and ability to provide practical, risk-based legal advice
  • Demonstrated ability to learn new subject matter quickly and translate complex legal concepts into practical business advice
  • Intellectual curiosity and interest in emerging technologies, AI, evolving regulatory frameworks, geopolitical and external factors
  • Ability to operate effectively in an increasingly global and interconnected environment involving cross-functional, cross-border, and multidisciplinary teams

Benefits

  • Health benefits
  • Life insurance
  • Disability benefits
  • 401(k) with company contribution and match
  • Vacation
  • Personal days
  • Holidays
  • Performance-based cash incentive
  • Annual equity awards

Company overview

Novartis is a global pharmaceutical company headquartered in Basel, Switzerland, dedicated to reimagining medicine to improve and extend people's lives. As an innovative medicines company, Novartis focuses on developing high-value treatments that address society's greatest disease burdens through technology leadership in research and development. The company operates across five core therapeutic areas: cardiovascular, renal and metabolic diseases; immunology; neuroscience; oncology; and hematology. With a workforce of approximately 75,883 employees worldwide, Novartis reaches nearly 300 million patients across 118 countries. The company leverages advanced technology platforms including targeted protein degradation, cell therapy, gene therapy, radioligand therapy, and xRNA to develop breakthrough treatments. Novartis maintains a strong portfolio of oncology drugs and generics while continuously expanding its pipeline through strategic acquisitions and internal research. The company's commitment extends beyond drug development to ensuring global access to medical innovations through novel access approaches and patient assistance programs.

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