Associate Director, Data Science

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 Summary This is a new position. You will join a cutting-edge Drug Development Data Science and Advanced Analytics (DSAA) team as a senior scientific and technical leader, driving data science strategy and execution to advance the global drug development process. We are looking for a seasoned data scientist with a strong computational, statistical, and biological background and a demonstrated track record of leading analytical strategy, driving methodological innovation, and translating complex, multi-modal data into impactful scientific insights that inform clinical development decisions. As an Associate Director, you will provide scientific leadership across diverse data types generated in drug development — including clinical trial data, genomics, proteomics, imaging, flow cytometry, and other biomarker modalities — driving both the strategic direction and hands‑on execution of data science efforts across early‑to‑late phase drug development programs. You will define and champion analytical frameworks, methodological standards, and scalable approaches that elevate the quality and impact of data science across the organization, while serving as a key scientific partner to Biostatistics leads, Translational and Clinical Scientists, and senior cross‑functional stakeholders. This position may include management of a small team of data scientists. We are looking for a technically excellent, scientifically influential, and strategically minded practitioner. What You’ll Do Data Science Strategy & Scientific Leadership Serve as a senior scientific resource within the DSAA organization, providing strategic direction and methodological guidance on data science approaches across multiple drug development programs Lead the design and execution of exploratory and confirmatory analyses (both hypothesis‑generating and hypothesis‑driven) across diverse and complex data types, from early discovery through late‑phase clinical development Drive the development and implementation of innovative statistical methods, novel analytical frameworks, and state‑of‑the‑art AI/ML approaches to address key scientific questions in drug development Shape the analytical strategy for drug development programs, contributing to decisions around trial design, endpoint selection, biomarker strategy, and evidence generation Identify opportunities to leverage emerging data science methodologies and technologies to accelerate drug development and address the complexities of novel data types Represent DSAA in cross‑functional program team meetings, providing authoritative scientific input and influencing development decisions through rigorous, data‑driven analysis Advanced Analytics & Modeling Lead the development and application of novel computational methods for patient segmentation, biomarker discovery, and precision medicine from multimodal clinical and omics datasets in partnership with Translational, Clinical, and Statistical Scientists Oversee and execute data science analyses on datasets from BMS clinical trials and real‑world data cohorts, spanning genomics, proteomics, imaging, flow cytometry, and other high‑dimensional biomarker data types Drive the integration, mining, and visualization of diverse, high‑dimensional, and disparate datasets across therapeutic areas and development phases, developing novel analytical approaches where existing methods fall short Lead the formulation, implementation, testing, and validation of predictive models and scalable automated processes for delivering modeling results across multiple programs Apply and advance the use of AI/ML, deep learning, NLP, causal ML, and explainable AI across multiple data modalities and clinical development contexts, maintaining currency with the state of the art Lead application of rigorous statistical approaches to clinical trial data, including survival analysis, longitudinal/mixed‑effects modeling, causal inference, and principled handling of missing data and censoring Contribute to and influence the scientific and statistical strategy of drug development programs, including the development of predictive biomarkers, novel trial designs, and precision medicine approaches Data Engineering & Reproducibility Define and champion standards for scalable, reproducible, and well‑documented analytical pipelines and codebases using Python, R, SQL, and cloud platforms Establish and enforce data quality frameworks to assess and ensure fitness‑for‑purpose of diverse data sources across programs Promote rigorous model evaluation practices including appropriate cross‑validation, calibration assessment, out‑of‑sample validation, and transparent reporting of model performance Drive adoption of scalable, automated analytical processes and best‑in‑class software engineering practices across the team Leadership, Mentorship & Cross‑Functional Influence If applicable, manage and develop a small team of data scientists, building capabilities, fostering scientific rigor and innovation, and ensuring delivery of high‑quality outputs within program timelines Mentor and provide technical guidance to junior and mid‑level data scientists, elevating team‑wide methodological and engineering standards through code reviews, collaborative problem‑solving, and knowledge sharing Partner with lead and protocol statisticians in shaping statistical analysis plans (SAPs) for exploratory data science analyses supporting drug development programs Collaborate with and influence cross‑functional teams including clinicians, translational medicine scientists, biostatisticians, data engineers, regulatory scientists, and IT/engineering professionals Communicate complex analytical strategies and results with clarity and scientific authority to both technical and non‑technical audiences, including senior leadership Build and maintain strong, high‑trust working relationships across the organization, establishing DSAA as a valued scientific partner Key Requirements Ph.D. in a relevant quantitative field (e.g., Computational Biology, Biostatistics, Statistics, Biomedical Engineering, Computer Science, or related field) and 6+ years of academic/industry experience; or Master's Degree in a relevant quantitative field and 8+ years of industry experience Demonstrated mastery in data science and statistical analysis with data generated from clinical trials or electronic health records, with a strong track record of delivering impactful results in a pharma R&D context Significant experience leading the development and application of statistical and machine learning models on high‑dimensional data for time‑to‑event, longitudinal, and multivariate outcomes Proven expertise in the application of AI/ML and proficiency in Python, R, SQL, and cloud platforms (e.g., AWS, Azure, Databricks) Deep familiarity with clinical trial design, drug development processes, and the role of biomarkers and data science in regulatory and clinical decision‑making Demonstrated ability to define and drive analytical strategy across multiple concurrent programs, balancing scientific rigor with practical delivery Significant track record of driving statistical and AI/ML innovation, with a perspective on leveraging emerging approaches to expedite drug development and address complexities of novel data types Demonstrated ability to lead, mentor, and collaborate with multidisciplinary teams, and to manage multiple concurrent high‑priority programs with competing timelines Excellent communication, data presentation, and visualization skills; ability to convey complex analytical concepts to diverse audiences including senior leadership Capable of establishing and sustaining strong, high‑trust working relationships across the organization Preferred Qualifications Experience with genomics, proteomics, imaging, flow cytometry, or immunobiology datasets from clinical trials is highly preferred Experience with NLP is highly preferred Experience with Survival Analysis and time‑to‑event modeling is highly preferred Experience with causal ML and explainable AI is highly preferred Knowledge of molecular biology and understanding of disease pathways is preferred Experience with real‑world data (RWD/RWE) sources, including EHR, claims, or registry data, and associated analytical and causal inference methods is preferred Familiarity with digital health data and wearable/sensor‑derived data types is a plus Experience with or exposure to novel clinical trial design (e.g., adaptive, platform, or biomarker‑enriched trials) is preferred Prior experience in a people management or formal scientific leadership role is a plus Experience with scalable compute and deployment patterns, including cloud‑based platforms and parallelization for large‑scale data processing and model training is a plus 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: $218,120 - $264,308Cambridge Crossing: $218,120 - $264,308Princeton - NJ - US: $189,670 - $229,834Seattle - WA: $208,640 - $252,824 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 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. 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 View email address on click.appcast.io . 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: 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 . 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 View email address on click.appcast.io . 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. R1605305 : Associate Director, Data Science Req Number: R1605305 Location: Princeton - New Jersey - US Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law. #J-18808-Ljbffr