Location: Uxbridge - GB
Time Type: Full time
Job Requisition ID: R1600843 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: the BMS careers website. Shape the Future of Drug Development
Are you a data science leader with the vision to transform complex, multi-modal data into life-changing scientific decisions? Bristol Myers Squibb is looking for an Associate Director of Data Science to join our cutting-edge Drug Development Data Science & Advanced Analytics (DSAA) team. This is a rare opportunity to operate at the intersection of advanced analytics, AI/ML innovation, and clinical science — driving both strategic direction and hands-on execution across early-to-late phase drug development programs. As a senior scientific and technical leader, you will define analytical frameworks, champion methodological standards, and serve as a key partner to cross-functional stakeholders across the organization. What You'll Do
Data Science Strategy & Scientific Leadership
Required Qualifications:
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 meeveem.com. Visit the BMS EEO accessibility page to access our complete Equal Employment Opportunity statement. Bristol Myers Squibb is Disability Confident – Employer. A UK Government scheme. Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. 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 the BMS fraud protection page. 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 meeveem.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.
Time Type: Full time
Job Requisition ID: R1600843 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: the BMS careers website. Shape the Future of Drug Development
Are you a data science leader with the vision to transform complex, multi-modal data into life-changing scientific decisions? Bristol Myers Squibb is looking for an Associate Director of Data Science to join our cutting-edge Drug Development Data Science & Advanced Analytics (DSAA) team. This is a rare opportunity to operate at the intersection of advanced analytics, AI/ML innovation, and clinical science — driving both strategic direction and hands-on execution across early-to-late phase drug development programs. As a senior scientific and technical leader, you will define analytical frameworks, champion methodological standards, and serve as a key partner to cross-functional stakeholders across the organization. What You'll Do
Data Science Strategy & Scientific Leadership
- Serve as a senior scientific resource within DSAA, providing strategic direction and methodological guidance across multiple drug development programs
- Lead the design and execution of exploratory and confirmatory analyses across diverse and complex data types — from early discovery through late-phase clinical development
- Shape analytical strategy for drug development programs, contributing to decisions around trial design, endpoint selection, biomarker strategy, and evidence generation
- Represent DSAA in cross-functional program team meetings, providing authoritative scientific input and influencing development decisions through rigorous, data-driven analysis
- Lead the development and application of novel computational methods for patient segmentation, biomarker discovery, and precision medicine from multimodal clinical and omics datasets
- Drive the integration, mining, and visualization of diverse, high-dimensional datasets across therapeutic areas and development phases — including genomics, proteomics, imaging, and flow cytometry
- Apply and advance the use of AI/ML, deep learning, NLP, causal ML, and explainable AI across multiple data modalities and clinical development contexts
- Lead application of rigorous statistical approaches to clinical trial data, including survival analysis, longitudinal/mixed-effects modelling, causal inference, and principled handling of missing data
- 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 ensure fitness-for-purpose of diverse data sources across programs
- Drive adoption of scalable, automated analytical processes and best-in-class software engineering practices across the team
- Manage and develop a small team of data scientists, building capabilities and fostering scientific rigor and innovation
- Mentor 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
- Communicate complex analytical strategies and results with clarity and scientific authority to both technical and non-technical audiences, including senior leadership
Required Qualifications:
- PhD in a relevant quantitative field (e.g., Computational Biology, Biostatistics, Statistics, Biomedical Engineering, or Computer Science) with 6+ years of academic/industry experience; or a Master's Degree in a relevant quantitative field with 8+ years of industry experience
- Demonstrated mastery in data science and statistical analysis using clinical trial or electronic health records data, 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 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
- Excellent communication, data presentation, and visualization skills with the ability to convey complex concepts to diverse audiences
- Experience with genomics, proteomics, imaging, flow cytometry, or immunobiology datasets from clinical trials
- Experience with NLP, causal ML, explainable AI, and survival analysis/time-to-event modelling
- Knowledge of molecular biology and understanding of disease pathways
- Experience with real-world data (RWD/RWE) sources, including EHR, claims, or registry data
- Familiarity with novel clinical trial designs (e.g., adaptive, platform, or biomarker-enriched trials)
- Prior experience in a people management or formal scientific leadership role
- Experience with cloud-based scalable compute and deployment patterns for large-scale data processing and model training
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 meeveem.com. Visit the BMS EEO accessibility page to access our complete Equal Employment Opportunity statement. Bristol Myers Squibb is Disability Confident – Employer. A UK Government scheme. Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. 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 the BMS fraud protection page. 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 meeveem.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.
Vacancy posted 5 days ago
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