Program Director Data Jobs in Needham, MA (NOW HIRING)

At Bristol Myers Squibb, our employees often ask, "Who are you working for?"-a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.

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
• 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

We hire for skills and capabilities, not just credentials - if this role excites you, but doesn't perfectly match your resume, we encourage you to apply anyway.

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully - carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

Benefits:

Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans - including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).

U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.

Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.

Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.

U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits

How We Work

Where you work matters - because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application, or in any part of the recruitment process, direct your inquiries toadastaffingsupport@bms.com. Visitcareers.bms.com/eeo-accessibilityto access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only: 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

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