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Director Cell Therapy Research Development Jobs

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Director Cell Therapy Research Development information

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$65.5K

$162.7K

$215K

How much do director cell therapy research development jobs pay per year?

As of Sep 10, 2026, the average yearly pay for director cell therapy research development in the United States is $162,707.00, according to ZipRecruiter salary data. Most workers in this role earn between $135,000.00 and $194,000.00 per year, depending on experience, location, and employer.

What does a director of cell therapy research development do?

A Director of Cell Therapy Research Development leads and manages research initiatives focused on developing new cell-based therapies, such as those used in cancer treatment or regenerative medicine. They oversee scientific teams, design research strategies, manage budgets, and ensure compliance with regulatory standards. This role also involves collaborating with clinical teams, regulatory agencies, and industry partners to advance therapies from the laboratory to clinical trials and ultimately to patients. Their leadership is crucial for driving innovation and ensuring that research projects meet both scientific and business objectives.

What are the key skills and qualifications needed to thrive as a director of cell therapy research development?

To thrive as a Director of Cell Therapy Research Development, you need advanced expertise in cellular biology, immunology, and drug development, typically supported by a PhD or MD and extensive experience in cell therapy research. Familiarity with regulatory requirements, Good Manufacturing Practice (GMP) standards, and laboratory management systems is crucial. Strong leadership, strategic vision, and the ability to communicate complex concepts clearly help drive innovation and collaboration across multidisciplinary teams. These skills ensure the successful development and translation of cell therapy products from research to clinical application, meeting both scientific and regulatory milestones.

What are some common challenges faced by a director of cell therapy research development, and how can they be addressed?

A Director of Cell Therapy Research Development often faces challenges such as managing cross-functional teams, navigating regulatory complexities, and ensuring the scalability of new therapies from research to clinical application. Addressing these challenges requires strong leadership, effective communication, and close collaboration with regulatory, clinical, and manufacturing partners. Staying current with industry trends and fostering a culture of innovation and compliance can also help overcome obstacles and drive successful project outcomes.

What is the difference between Director Cell Therapy Research Development vs Cell Therapy Research Scientist?

AspectDirector Cell Therapy Research DevelopmentCell Therapy Research Scientist
CredentialsAdvanced degrees (PhD, MD), extensive experience in cell therapyTypically a PhD or Master's in related fields
Work EnvironmentLeadership roles in R&D departments, strategic planningLaboratory research, experimental design, data analysis
Employer & Industry UsageBiotech and pharmaceutical companies, clinical research organizationsResearch institutions, biotech firms, academic labs
Search & Comparison IntentUnderstanding leadership roles, career progressionResearch activities, technical skills

The main difference between a Director Cell Therapy Research Development and a Cell Therapy Research Scientist lies in their responsibilities and experience level. The director oversees strategic planning, manages teams, and guides development projects, while the scientist focuses on conducting experiments and generating data. Both roles require strong expertise in cell therapy, but the director typically has more leadership and managerial duties.

What are popular job titles related to Director Cell Therapy Research Development jobs?

For Director Cell Therapy Research Development jobs, the most frequently searched job titles are:

Infographic showing various Director Cell Therapy Research Development job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 82% Full Time, 14% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $162,707 per year, or $78.2 per hour.

Senior Director, Cell Therapy WW Medical Affairs, Multiple Myeloma

Princeton, NJ • On-site

Bristol-Myers Squibb Company
Scientific Research and Development Services • 10K+ employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago


Bristol Myers Squibb rating

8.2

Company rating: 8.2 out of 10

Based on 51 frontline employees who took The Breakroom Quiz


Job description

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.
Position Overview
At BMS, we are committed to the advancement of science with the drive to improve every day for the benefit of patients. To accelerate our position as leaders in cell therapy and serve patients around the world, we are committed to being at the forefront of change.
Reporting to the Executive Director, Cell Therapy Multiple Myeloma, the Senior Director, WW Medical, Multiple Myeloma Cell Therapy will represent WW Medical Affairs as a therapeutic area expert and provide strategic scientific leadership for arlo-cel, our GPRC5D CAR T currently in clinical development in multiple myeloma. This individual will be accountable for driving global launch readiness, including external communications and market shaping, internal readiness, and strategic partnership on launch activities across the matrix. The role carries forward-looking responsibility across the broader MM Cell Therapy portfolio, including lifecycle management priorities and evidence generation strategy.
The role requires depth of scientific expertise, credibility with external thought leaders, and the leadership composure to operate effectively at the intersection of WW commercialization, local Medical Affairs, and global Clinical Development. This is a high-visibility, high-impact role at a pivotal moment in the evolution of BMS's Cell Therapy franchise, demanding an individual who can balance strategic vision with flawless operational execution in a complex, matrixed environment.
Key Responsibilities
Strategic Leadership of Arlo-cel
  • Lead WW Medical Affairs strategy for arlo-cel, driving global launch readiness across external communications, market shaping, and internal readiness activities
  • Lead cross-functional initiatives related to arlo-cel, integrating strategies across the MM portfolio where necessary
  • Collaborate with local Medical Affairs teams to align on launch strategy and tactics, ensuring cohesive, market-ready action plans globally
  • Drive cross-asset collaboration and knowledge sharing, fostering a unified BMS presence in multiple myeloma, including partnerships across Cell Therapy and Oncology
  • Establish and cultivate relationships with key thought leaders and KOLs at major academic centers; engage cooperative groups, steering committees, and advisory boards to generate insights and shape the evolving treatment paradigm

Seamless Execution of Core Medical Affairs Deliverables
  • Provide strategic input to guide publication planning and execution; serve as a key reviewer on abstracts, presentations, and publications
  • Develop and implement congress strategies to achieve impactful scientific presence and engagement at major meetings including COMy, EHA, and IMS
  • Provide strategic input into BMS-sponsored symposia and independent medical education events to enhance scientific dialogue
  • Refine the Integrated Evidence Plan (IEP) to ensure alignment with cross-functional goals; provide strategic input for evidence generation projects, including expert review and recommendations for new ISR and CRC trials as well as HEOR analyses
  • Represent arlo-cel as a leading member of the WW MM Asset Indication Medical Strategy (AIMS) team to ensure the global Medical Affairs strategy and deliverables are aligned across key medical functions and markets
  • Conduct comprehensive reviews of publications and update key launchpad assets, including slide decks, training sessions, and Q&A materials
  • Ensure scientific excellence in medical education and effective data exchange

Provide Scientific/Medical Expertise Across the Matrix
  • Offer medical insights to guide clinical development plans and influence strategic decision-making for both early and late development, including knowledge sharing across assets in the BMS pipeline
  • Serve as subject matter expert to cross-functional partners in multiple myeloma, providing guidance that drives scientific and commercial priorities
  • Collaborate with global and local market access and marketing teams, providing expert medical content to support key initiatives
  • Work collaboratively with patient advocacy to align objectives and enhance engagement

Qualifications & Experience
  • Advanced degree (MD, PhD, or PharmD) required; strong background in oncology/hematology, cell biology, or a related life sciences discipline preferred
  • 8-10+ years of pharmaceutical industry experience required; Medical Affairs experience required; experience in multiple myeloma required; CAR-T or cell therapy experience strongly preferred
  • Demonstrated launch experience; CAR-T or cell therapy launch experience is a significant differentiator
  • Familiarity with clinical and translational research activities and the drug development process
  • Proven track record of operating effectively within complex, matrixed WW and cross-functional organizations; demonstrated ability to influence without authority and build alignment across diverse stakeholders
  • Strategic thinking: demonstrated ability to synthesize complex inputs, perform strategic assessments, and develop clearly framed choices and recommendations with measurable accountability for outcomes
  • Cross-functional experience: highly collaborative, with a record of building and maintaining cross-functional relationships and communicating effectively with senior leadership, peers, and external experts
  • Excellent verbal and written communication skills, including presentations to large groups, senior leadership, interactive scientific discussions, and 1:1 engagement with thought leaders
  • Interpersonal skills: ability to build relationships, influence, and drive organizational engagement at all levels
  • Proven agility in prioritizing and navigating competing demands in a deadline-driven environment
  • Estimated 20-30% domestic and international travel (as applicable)

#LI-HYBRID
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Compensation Overview:
Madison - Giralda - NJ - US: $229,380 - $277,956Princeton - NJ - US: $229,380 - $277,956
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
  • Health Coverage: Medical, pharmacy, dental, and vision care.
  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.

Work-life benefits include:
Paid Time Off
  • US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
  • Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science™ ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1604746 : Senior Director, Cell Therapy WW Medical Affairs, Multiple Myeloma

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About Bristol-Myers Squibb

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Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.

Industry

Scientific research and development services and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US