E.R. Squibb & Sons,L.L.C. Posted August 20, 2026

Senior Manager, Data Science

Warsaw-WeWork-PL, Poland Full time
Clinical Development Manager

E.R. Squibb & Sons,L.L.C. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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 .

Senior Manager, Data Science

Department: Data Science and Advanced Analytics (DSAA)

Position Summary

This is a new position. You will join a cutting-edge Drug Development Data Science and Advanced Analytics (DSAA) team to advance the global drug development process. We are looking for a candidate with strong computational, statistical, and biological capabilities and a demonstrated track record of translating complex, multi-modal data into testable hypotheses and actionable insights in support of clinical development activities and decisions.

As a hands-on individual contributor, you will drive exploratory and confirmatory analyses (both hypothesis-generating and hypothesis-driven) across diverse data types generated in drug development, including clinical trial data, genomics, proteomics, imaging, flow cytometry, and other biomarker modalities. You will define and implement approaches, processes, algorithms, and pipelines that support the analytics, visualization, and decision support needs of drug development scientists and project teams, while collaborating closely with Biostatistics leads, Translational and Clinical Scientists, and cross-functional partners across the organization. We are looking for a hands-on, state-of-the-art practitioner.

What You'll Do

Data Science & Analytics

Develop and apply novel or existing computational methods for patient segmentation, biomarker discovery, and hypothesis generation from multimodal clinical and omics datasets in partnership with Translational, Clinical, and Statistical Scientists

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

Develop novel ways of integrating, mining, and visualizing diverse, high-dimensional, and disparate datasets generated across early-to-late phase drug development

Formulate, implement, test, and validate predictive models and implement efficient automated processes for producing modeling results at scale

Perform relevant and innovative statistical analyses of high-dimensional data (e.g., gene expression, sequencing, imaging features) generated by cutting-edge technologies

Apply modern machine learning capabilities, including AI/ML, deep learning, NLP, causal ML, and explainable AI, across multiple data modalities and clinical development contexts

Apply statistically rigorous approaches to clinical trial data, including survival analysis, longitudinal/mixed-effects modeling, and appropriate handling of missing data and censoring

Contribute to 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

Build and maintain well-structured, reproducible, version-controlled analytical pipelines and codebases using Python, R, SQL, and cloud platforms

Develop and apply data quality frameworks to assess and ensure fitness-for-purpose of diverse data sources for specific analytical questions

Implement strong evaluation practices including appropriate cross-validation strategies, calibration assessment, and transparent reporting of model performance and limitations

Build scalable, automated processes for delivering analytical results across multiple programs and data types

Collaboration & Technical Contribution

Partner with lead and protocol statisticians in contributing to statistical analysis plans (SAPs) for exploratory data science analyses supporting drug development programs

Collaborate with cross-functional teams including clinicians, translational medicine scientists, biostatisticians, data engineers, and IT/engineering professionals

Contribute to team excellence via code reviews, technical mentorship, and raising the overall engineering and methodological rigor of the team

Communicate analytical results clearly and effectively to both technical and non-technical stakeholders, with strong data presentation and visualization skills

Manage and coordinate resources to produce quality deliverables within timelines for competing priorities

Build and maintain strong working relationships across the organization

Key Requirements

Ph.D. in a relevant quantitative field (e.g., Computational Biology, Biostatistics, Statistics, Biomedical Engineering, Computer Science, or related field) and 1+ years of academic/industry experience; or Master's Degree in a relevant quantitative field and 3+ years of industry experience

Strong experience in data science and statistical analysis with data generated from clinical trials or electronic health records, particularly in application to pharma R&D

Experience in developing and validating statistical and machine learning models on high-dimensional data for time-to-event, longitudinal, and multivariate outcomes

Experience in the application of AI/ML and proficiency in Python, R, SQL, and cloud platforms (e.g., AWS, Azure, Databricks)

Familiarity with clinical trial design, drug development processes, and the role of biomarkers in regulatory and clinical decision-making

Perspective in leveraging innovative approaches to expedite drug development and address the complexities of emerging data

Ability to work both independently and collaboratively, and to handle several concurrent, fast-paced projects

Strong problem-solving and collaboration skills, and rigorous and creative thinking

Excellent communication, data presentation, and visualization skills

Capable of establishing strong 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 and associated analytical methods is preferred

Familiarity with digital health data and wearable/sensor-derived data types 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:

Warsaw - PL: zł354,470 - zł429,541


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 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. The final compensation will be determined based on demonstrated experience and in accordance with pay equity principles and applicable employment laws.

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.

R1605256 : Senior Manager, Data Science

Job details

Seniority
Manager
Function
Clinical Development
Therapeutic area
Not listed
Location
Warsaw-WeWork-PL, Poland
Employment type
Full time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 363 comparable Manager Clinical Development roles across 57 biopharma companies.

363Comparable roles tracked
334Currently active
57Companies hiring similar roles
32Countries represented

Salary context

106 of 363 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Patient Safety Epidemiology Associate Director · Vertex Pharmaceuticals Inc (US) $0/hr – $0/hr (≈ $0–$0/yr)
Highest disclosed · Statistical Advisor · Gilead Sciences, Inc. $226,185/yr – $292,710/yr
Peer group range $0 – $259,448 (median $169,700)

Where these roles are based

Top locations among the 363 comparable roles

United States164
India65
United Kingdom23
Poland19
China12
Germany10

+ 26 more countries

Seniority mix

363 of 363 peers have a known seniority level

Manager203
Associate Director102
Associate58

Therapeutic area mix

37 of 363 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology14
Immunology10
Cardiovascular / CVRM6
Neuroscience4
Dermatology & Aesthetics2
Ophthalmology1

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The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.