R&D BI&T Associate Director, Clinical Pharmacology and Pharmacometrics en Bristol Myers Squibb
Bristol Myers Squibb · Princeton, Estados Unidos De América · Onsite
- Professional
- Oficina en Princeton
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.
Summary:
The Research BI&T Clinical Pharmacology and Pharmacometrics Product Owner is accountable for end-to-end technical delivery and lifecycle management of applications, data, and platforms serving Clinical Pharmacology and Pharmacometrics. This is a hands-on role to deliver seamless integration, enhancement, and operational excellence of systems enabling PK/PD modeling, statistical analysis, and scientific workflows. This role drives technical strategy, partners cross-functionally, and leads empowered teams to deliver innovative solutions that keep our research ecosystem at the cutting edge.
Key Responsibilities
Technical Delivery & Integration:
Accountable for the delivery, enhancement, and lifecycle management of modeling/simulation tools (e.g., R, NONMEM, Monolix, Python, PsN, Pirana, SAS, JupyterHub).
Lead integration projects across internal IT (LDAP, AWS, Info Security, Scientific Computing Services) and external vendors (Metrum, Simulations Plus, PumasAI/JuliaHub).
Ensure validated systems compliance and effective application lifecycle management.
Design, build, and deploy GenAI applications and agentic workflows, including hands-on fine-tuning, evaluation, and operationalization of LLMs and deep learning models for scientific and operational applications.
Collaborate with scientists and stakeholders to identify and scope impactful GenAI use-cases, translating business and scientific requirements into robust machine learning solutions.
Team Leadership & Stakeholder Engagement:
Lead and coach a dedicated full-stack delivery team (analysts, engineers, testers, scrum masters).
Partner with business stakeholders, Product Owners, and cross-functional leaders to translate scientific requirements into technical solutions.
Set goals, prioritize work, and foster a high-performance culture aligned with organizational NorthStar outcomes.
Accountable for CP&P Roadmap and reporting in collaboration with Research and BI&T Partners.
Strategic Proactivity & Innovation:
Anticipate emerging needs in pharmacometrics and proactively pilot and scale new capabilities (AI/ML and GenAI integration, cloud migration, enhanced data findability).
Drive continuous improvement and adoption of future-defining technologies, including GenAI, that advance research strategy.
Operational Excellence:
Ensure robust documentation, system administration, and support for Linux/HPC environments.
Manage AWS environments (Parallel Cluster, Kubernetes), version control (SVN/GitHub), and custom scripting (shell, Python).
Maintain strong vendor relationships and monitor product/service roadmaps.
Responsible for Product portfolio license management and budgeting
Required Experience:
5-8 years’ experience in IT delivery or applications development, preferably supporting scientific or pharmaceutical domains.
Proven track record managing complex integrations, validated systems, and cloud-based platforms (AWS/Azure).
Strong knowledge of Unix/Linux, HPC grid (SGE/Slurm), shell scripting, and R package management.
Experience leading agile teams and delivering projects using Agile, Scrum, or Kanban methodologies.
Excellent documentation, communication, and stakeholder management skills.
Bachelor’s or graduate degree in Computer Science, Information Technology, Pharmaceutical Sciences, or equivalent experience.
Familiarity with pharmaceutics modeling and simulation tools, scientific workflow optimization, and AI/ML/GenAI application in research.
Key Leadership & Operating Behaviors:
Strategic proactivity and bias to action—anticipates needs, starts pilots, and scales solutions.
Outcome obsession—drives measurable impact for patients and research colleagues.
Cross-functional versatility—forms empowered teams and simplifies handoffs.
Recognized expertise—counsel sought on complex topics; delivers high-quality products.
Innovation—defines the future, experiments, and scales new capabilities.
Talent multiplication—develops successors and fosters candid feedback rhythms.
Key Stakeholder Groups:
Quantitative Pharmacology & Pharmacometrics Scientists
Internal IT and Scientific Computing Teams
External Vendors and Technology Partners
Research Leadership and Cross-Functional Product Owners
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:
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 https://careers.bms.com/life-at-bms/.
Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year’s holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition 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.
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 [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
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/
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
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