Title: Associate Director, Global Clinical Scientist (Cell Therapy) Location: Princeton United States time type Full time job requisition id R1603544 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. The Associate Director, Global Clinical Scientist provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective - Responsible for implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical Trial Lead for one or more trials - Successfully leads, plans, and executes trial level activities for multiple trials with minimal to moderate level of supervision - Provides scientific and clinical leadership to team of supporting Clinical Scientists (matrix leadership) - Co-Leads study team meetings in partnership with GDO protocol manager; and collaborate with cross functional study team members - May support clinical development planning (collaboration with Clinical Development Lead/Clinical Trial Physician for provision and analysis of data to support future planning) Position Responsibilities - Maintain a thorough understanding of assigned protocols and protocol requirements; educate supporting team members - Plan and lead the implementation all study startup/conduct/close-out activities as applicable - Evaluate innovative trial designs (collaboration with Medical Monitor/Clinical Development Lead) - Protocol and ICF development process with minimal guidance; including writing, reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality (collaboration with Medical Writing) - Site-facing activities such as training and serving as primary contact for clinical questions - Activities related to data generation and validation, including CRF design, clinical data review/query resolution; ensure consistent, quality data review by supporting CS team - Clinical data trend identification; provide trends and escalate questions to Medical Monitor - Develop clinical narrative plan; review clinical narratives - Provision of information required by Protocol Manager for development of trial budget, CRO scope of work, etc. - Review development of site and CRA training materials and presentation at SIV and Investigator meetings and support on Study committee (e.g., DMC) activities - Drafting/review and validation of clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, regulatory responses) - Collaborate and serve as primary liaison between external partners for scientific advice Degree Requirements - Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred) Experience Requirements - 5+ years of experience in clinical science, clinical research, or equivalent - Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations - Proficient knowledge and skills to support program specific data review, trend identification, data interpretation - Knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees Key Competency Requirements - Excellent verbal, written, communication and interpersonal skills - Must be able to effectively communicate and collaborate across functions and job levels - Ability to assimilate technical information quickly - Routinely takes initiative - Detail-oriented - Strong sense of teamwork; ability to lead team activities - Proficient in Medical Terminology and medical writing skills - Proficient knowledge of the disease area(s), KOLs, indication(s), compound(s) under study (including MOA, PK/PD, biomarker & safety profile) - Proficient critical thinking, problem solving, decision making skills - Understanding of functional and cross-functional relationships - Commitment to Quality - Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalism - Proficient planning/project management skills (ability to develop short to mid-range plans that are realistic and effective in meeting goals) - Proficient in Microsoft Word, Excel, PowerPoint, Electronic Data Capture (e.g., RAVE), J-Review or similar data reporting tools Travel Required Domestic and International travel may be required. 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: Brisbane - CA - US: $211,910 - $256,789 Madison - Giralda - NJ - US: $184,270 - $223,294 Princeton - NJ - US: $184,270 - $223,294 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. 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.

Lead and manage clinical development strategies, ensuring alignment with regulatory goals, while mentoring clinical trial physicians and overseeing the execution and analysis of clinical studies across multiple indications.

Lead prospect research and portfolio management to optimize donor engagement, develop strategic partnerships, and implement data-driven decision-making while fostering team growth and aligning cross-functional stakeholders with organizational goals.

• Manage our strategy, grounded in data analysis and empirical thoughtfulness • Use Python and SQL to independently explore datasets, validate hypotheses, and surface unique insights • Translate analytical findings, model outputs, and product capabilities into clear, market‑facing narratives that demonstrate value • Develop industry perspectives on credit lifecycle optimization, alternative data, machine learning adoption, portfolio risk, fraud, and regulatory trends • Support large strategic sales opportunities with analytical framing, benchmarks, and data‑driven proof points that strengthen value propositions • Create executive‑ready content—including industry reports, white papers, sales enablement decks, client POVs, and conference presentations • Collaborate with Data Science teams to validate assumptions, interpret model behavior, and ensure analytical rigor in published insights • Identify new industry trends using both qualitative indicators and quantitative evidence • Represent us externally, presenting Experience researching and generating leads grounded insights to senior client and industry audiences