Jobs · Business Development · Massachusetts

Executive Director, In Vivo Cell Therapy Innovation, Cell Therapy Thematic Research Center

Bristol Myers Squibb EU Policy · Cambridge, MA · 1 wk ago
On-siteBusiness Development$285k–$345k/yrFull-time

Position Summary

The Executive Director will lead a high-performing team of scientists to advance innovative therapeutic strategies in non-viral in vivo cell engineering. This role is responsible for driving the discovery and early development of next-generation in vivo cell therapy drug candidates, with a focus on translating cutting-edge science into impactful clinical and business outcomes.

Position Responsibilities

  • Applies leading-edge and significant knowledge of cell therapy engineering and gene editing principles in to lead highly complex projects involving multi-disciplinary groups and external parties/organizations

  • Recognized as an influential authority across the company and in the external scientific community in the fields of gene editing, cell therapy, and in vivo therapeutic modalities

  • Recognizes and champions programs and initiatives to support strategic research goals and direction across multiple disciplines and capabilities within the in vivo therapy space

  • Delivers results that have a measurable impact on company performance strategically, financially, and operationally — translating cutting-edge science into viable therapeutic programs

  • Serves as a subject matter expert providing strategic and functional guidance across cell-based therapeutic approaches, gene editing platforms, and non-viral delivery systems

  • Affected by the external community — including academic institutions, biotech partners, and industry consortia

  • Actively involved in initiatives that encourage and develop scientific capability in others, fostering the next generation of in vivo therapy researchers

Experience

  • Basic Qualifications: Master’s Degree or Ph.D. in the Life Sciences with 20+ years of academic and/or industry experience

  • Preferred Qualifications: Extensive expertise in gene editing technologies, extensive experience leading and developing teams of scientists, strong publication and/or patent record, familiarity with regulatory frameworks relevant to gene editing and in vivo therapies

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