5 дней назад
Executive Director, Global Program Leader (In Vivo CAR-T)
256 073 - 336 097$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Executive Director, Global Program Leader (in vivo CAR-T/biotechnology): Leading the strategy, execution, and governance of global in vivo CAR-T development programs from IND-enabling studies through clinical proof-of-concept, registration, and lifecycle management with an accent on cross-functional leadership, regulatory strategy, and portfolio decisions. Focus on designing global development plans, resolving strategic and operational risks, and advancing cell and gene therapies through major clinical and regulatory milestones.
Location: Hybrid role based in Somerset, New Jersey, United States. Applicants must be authorized to work in the United States.
Base pay: $256,073–$336,097 USD per year, plus performance-based bonus and/or equity for eligible roles.
Company
is a commercial-stage biotechnology company developing cell therapy platforms, including CAR-T, CAR-NK, CAR-γδ T, and in vivo genetic medicine approaches for serious diseases.
What you will do
- Lead the strategy and execution of in vivo CAR-T programs across the full development lifecycle.
- Develop integrated global plans covering scientific, clinical, regulatory, manufacturing, commercial, financial, and operational objectives.
- Chair Global Program Teams and coordinate Research, Clinical Development, Regulatory Affairs, Translational Sciences, CMC, Quality, Manufacturing, Commercial, Finance, and Business Development.
- Drive portfolio decisions by evaluating benefit-risk profiles, competitive landscapes, investment priorities, development scenarios, and milestones.
- Guide regulatory interactions and readiness for IND, CTA, BLA/MAA, registration, and lifecycle management activities.
- Present program strategies and risks to executive leadership while mentoring cross-functional program members and managing strategic contingencies.
Requirements
- 10+ years of biotechnology or pharmaceutical industry experience in drug development.
- 5+ years of leadership experience managing complex global development programs.
- Demonstrated success advancing biologics, cell therapies, gene therapies, or other advanced therapeutic programs through clinical development.
- Experience leading cross-functional teams in a matrix environment and supporting global regulatory interactions and major submissions.
- Strong knowledge of cell and gene therapy development, including emerging in vivo CAR-T technologies, global clinical development, and registration pathways.
- United States work authorization is required; employment eligibility is verified through E-Verify.
Nice to have
- Experience in oncology, immunology, cell therapy, gene therapy, or in vivo genetic medicines.
Culture & Benefits
- Hybrid work environment within a global biotechnology organization.
- Medical, dental, and vision insurance with a 401(k) plan and company match.
- Eight weeks of paid parental leave after three months of employment.
- Paid vacation, personal and sick time, floating holidays, and eleven company holidays.
- Additional flexible spending, health savings, disability, life insurance, family planning, well-being, and commuter benefits.
- Benefits are available exclusively to permanent full-time employees; contractors are not eligible.
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