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Director Regeneron Jobs (NOW HIRING)

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Global Procurement Direct to join our team supporting our ...

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What does a director at Regeneron do?

A Director at Regeneron is a senior leadership role responsible for overseeing teams or departments within the company, which specializes in biotechnology and pharmaceutical research. Directors typically manage strategic planning, project execution, and team leadership to ensure successful delivery of objectives in areas like research, clinical development, manufacturing, or corporate functions. They collaborate with other leaders to align their department's goals with the company's mission and growth. Additionally, Directors are involved in mentoring staff, budget management, and ensuring regulatory compliance in their respective areas.

What are the key skills and qualifications needed to thrive as a director at Regeneron, and why are they important?

To thrive as a Director at Regeneron, you need a strong background in life sciences or biotechnology, leadership experience, and a proven track record of driving strategic initiatives, typically supported by an advanced degree (PhD, MD, or MBA). Familiarity with regulatory compliance, project management tools, and industry-standard software platforms is crucial. Outstanding interpersonal skills, strategic thinking, and the ability to inspire cross-functional teams help set top performers apart. These skills ensure effective leadership, innovation, and successful execution of complex projects in a fast-paced biopharmaceutical environment.

What are some common challenges faced by a director at Regeneron, and how can they be addressed?

Directors at Regeneron often navigate the complexities of leading cross-functional teams in a fast-paced, innovative environment. Common challenges include balancing strategic oversight with hands-on project management and ensuring alignment between diverse departments such as research, clinical development, and regulatory affairs. Effective communication, adaptability, and a collaborative leadership style are essential to address these challenges. Directors are encouraged to foster open dialogue, set clear priorities, and leverage internal training resources to stay current with industry best practices.
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Infographic showing various Director Regeneron job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, 1% Temporary, and 1% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Head of Regeneron Cell Medicines

Regeneron Pharmaceuticals, Inc (USA)

Cambridge, MA • On-site

$180 - $230/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 28 days ago


Regeneron rating

8.5

Company rating: 8.5 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

19th of 86 rated pharmaceutical


Job description

Head of Regeneron Cell Medicines

Location: Cambridge, MA (primary site)

The Head of Regeneron Cell Medicines (RCM) sets the vision, strategy, and execution for Regeneron’s cell medicines portfolio and technology platform. The role spans ex vivo and in vivo CART programs and enabling technologies for delivery, including chemo‑free conditioning. This senior scientific executive oversees cross‑functional initiatives from discovery through early clinical development, builds and mentors high‑performing teams, and partners across the enterprise and with external collaborators to deliver transformative cell‑based therapies.

Responsibilities

Strategy and Portfolio Leadership

Define and drive the long‑term scientific vision and portfolio strategy for ex vivo and in vivo cell medicines, aligned to enterprise priorities. Prioritize programs and platform investments using data‑driven governance, scenario planning, and risk/benefit frameworks. Champion innovation in cell engineering, in vivo delivery (e.g., LNPs, viral vectors), and manufacturing to create differentiated therapies.

Scientific Program Oversight

Lead matrixed teams to deliver milestones from target validation to IND, PhaseI manufacturing, and early clinical readouts. Guide technical problem solving across modalities, including CART design, delivery optimization, biodistribution/PK, on/off‑target assessment, and safety risk mitigation. Integrate enabling platforms where justified.

People Leadership and Organizational Development

Build, mentor, and retain a diverse, high‑performing organization of senior scientific leaders and functional experts. Foster a culture of scientific excellence, accountability, collaboration, and inclusion across sites and functions. Implement succession planning, talent development, and performance management.

Cross‑Functional and Cross‑Site Collaboration

Partner closely with Research, Preclinical Development, Clinical, Regulatory, Quality, CMC, Manufacturing, BD, and Finance. Coordinate with vector/delivery, immunology, and translational biomarker teams to accelerate RCM programs to clinical evaluation.

External Innovation and Partnerships

Identify and evaluate external opportunities (academia, biotech, consortia, platforms) to accelerate the pipeline and capabilities. Negotiate and govern collaborations to clear, value‑creating outcomes.

Operational Excellence and Compliance

Own budgets, headcount planning, and resource allocation across programs and platform functions. Ensure adherence to biosafety, ethical guidelines, and regulatory standards (e.g., IND enabling, GxP interfaces). Drive reproducibility, data integrity, and robust decision records.

Executive Communication and Governance

Provide clear, concise updates to executive leadership and governance bodies on strategy, progress, risks, and mitigation plans. Represent Regeneron Cell Medicines at internal and external forums, scientific conferences, and with partners.

Qualifications and Experience

Advanced degree (PhD, MD, or MD/PhD) in cell biology, immunology, bioengineering, or a related discipline. 20+years of biopharmaceutical R&D experience with a substantial focus on cell‑based therapies; a proven track record advancing programs from discovery to IND and early clinical trials. Demonstrated leadership of multidisciplinary, multisite teams and senior people leaders in a fast‑paced environment. Deep expertise across key domains: cell engineering (CAR design, viral vectors), potency/identity assays, process and analytical development, and translational biology. In‑vivo gene delivery experience for CART, including viral and non‑viral modalities (LVV, LNPs), tissue/cell targeting strategies, biodistribution/PK, on/off‑target risk assessment, and immunogenicity management. CMC considerations for in‑vivo modalities versus exvivo products. Familiarity with regulatory pathways for cell and gene therapies (FDA/EMA guidance, IND preparation, RMAT considerations), including in‑vivo gene therapy non‑clinical packages (biodistribution, toxicology, shedding). Strong portfolio management, resource planning, and financial acumen. Exceptional communication, influence, and stakeholder management; effective in executive forums and cross‑functional decision making. Commitment to building an inclusive culture and developing talent.

Benefits

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (medical, dental, vision, life and disability), paid time off, and family support benefits.

Equal Employment Opportunity

Regeneron is an equal‑opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief, sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, Regeneron will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

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