Senior Director, Clinical Pharmacology & Pharmacometrics, Research Business Insights & Technology

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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: Overview

Bristol Myers Squibb is seeking a strategic scientifically grounded leader to serve as the Senior Director for Clinical Pharmacology & Pharmacometrics. This leader will partner deeply with Clinical Pharmacology Pharmacometrics Quantitative Pharmacology and Translational Medicine stakeholders to deliver the applications modeling environments workflow automation and governed operational capabilities that support CPP work end to endfrom quantitative preclinical-to-clinical bridging through clinical PK/PD dose and regimen decisions and submission-support outputs.

This role supports the quantitative CPP layer across Research and Development including pharmacometric workflows clinical PK/PD systems modeling platforms reporting automation regulatory evidence generation and the governed operational capabilities required to run these workflows at scale.

Reporting to the Vice President Research Business Insights & Technology this leader will operate as part of a unified BI&T leadership team and act as a trusted partner to Research and Development leadership. The role carries accountability for the reliability fit-for-purpose evolution and long-term scaling of the CPP technology stack and workflow ecosystem while working in a highly matrixed model with scientific leaders data teams lab-platform teams and regulatory-facing partners.

Mission & Impact

• Provide a scalable application and workflow backbone for CPP across preclinical-to-clinical translation clinical PK/PD dose selection exposure-response and model-informed development decisions

• Improve the speed quality reproducibility traceability and inspection-readiness of pharmacometrics and clinical pharmacology workflows

• Strengthen regulatory submissions through robust reporting reusable quantitative evidence generation and auditable outputs that support documents such as clinical pharmacology summaries and model-based appendices

• Enable governed automation of priority CPP workflows including reporting simulation execution review and knowledge reuse

• Create a durable technology foundation for end-to-end CPP that can scale with pipeline demand and integrate cleanly across the broader Research and Development ecosystem

Sub-Areas in Scope

• Clinical pharmacology and pharmacometrics applications including population PK PK/PD exposure-response dose optimization and model-informed decision support

• PBPK QSP drug-drug interaction and other quantitative modeling environments used in CPP workflows

• Clinical PK/PD systems and operational tooling that support end-to-end CPP execution

• CPAR Quarto-based or similar reporting automation and submission-support workflows for quantitative regulatory deliverables

• Quantitative translational workflows that bridge preclinical and clinical evidence in support of CPP decision-making

• Workflow governance audit trails validation support access controls and inspection-ready operational practices for regulated quantitative environments

• AI-enabled and advanced analytics capabilities that improve CPP workflow efficiency simulation review reporting and knowledge reuse

• In partnership but not sole ownership: translational labs pathology molecular and imaging lab workflows CLIA-oriented lab operations precision medicine diagnostics and broad bioanalytical capabilities

Key Responsibilities

• Serve as the single BI&T point of accountability for CPP technology applications workflows and support services end to end

• Partner across Research and Development to integrate CPP workflows with the scientific data and operational capabilities required for model-informed drug development

• Own clinical pharmacology and pharmacometrics applications modeling environments reporting workflows and operational support for core CPP use cases

• Ensure operational excellence reliability governance and continuous improvement across modeling environments clinical PK/PD systems reporting workflows and submission-support applications

• Lead automation of priority CPP workflows including model execution reporting simulation traceability review and evidence reuse

• Support quantitative regulatory deliverables through fit-for-purpose tooling reproducible workflows and inspection-ready practices

• Partner with Unified Lab & Experimental Platforms Target & Disease Biology and In-Vivo & Non-Clinical Pharmacology where translational science lab systems diagnostics biomarker workflows or bioanalytical capabilities intersect with CPP needs

• Partner with the R&D Data organization on underlying data-product strategy integration and fit-for-purpose data access

• Lead and grow a team of scientific technologists product leaders and specialized engineers aligned to this domain

Required Experience & Qualifications

• Ph.D. in Pharmacometrics Clinical Pharmacology Pharmaceutical Sciences Biostatistics or related quantitative field

• 12 years in pharmaceutical R&D with deep clinical pharmacology pharmacometrics and model-informed drug development experience

• Proven experience implementing or leading CPP applications PBPK and QSP environments clinical PK/PD systems or quantitative workflow automation

• Demonstrated experience supporting regulatory submissions quantitative reporting and governed workflows in Development-facing settings

• Experience applying AI/ML or advanced automation to quantitative modeling reporting or regulated scientific workflows is preferred

• Director or Senior Director-level leadership experience; experience building and scaling a specialized scientific technology team is a strong differentiator

Critical Capabilities

• Scientific Depth in Clinical Pharmacology and Pharmacometrics Deep credibility with quantitative scientists and domain leaders across CPP

• Strategic Partnership Translates scientific and Development needs into practical integrated technology and workflow solutions

• Operational Leadership Builds reliable scalable inspection-ready environments and support models for critical quantitative workflows

• Regulatory Translation Capability Understands how quantitative evidence is prepared reported reviewed and used in regulatory settings

Leadership & Change Attributes

• Strong partnership with senior scientific clinical and regulatory leaders

• Comfort operating with regulatory and global Development stakeholders

• Ability to recruit develop and retain highly specialized quantitative talent in a competitive market

• Experience navigating matrixed organizations and building credibility quickly

• Commitment to building a collaborative high-performing culture in a growing team

What Differentiates Top Candidates

• Experience as a clinical pharmacology or pharmacometrics technology leader inside a top-tier pharmaceutical R&D organization

• Track record of applications workflows or platforms that improved dose selection quantitative decision-making or regulatory execution in Development-facing settings

• Experience deploying workflow automation AI-enabled capabilities or advanced analytics in support of end-to-end CPP modeling reporting and decision-support operations

• Demonstrated success building a specialized function from foundational capability to scaled organizational value while operating through strong matrix partnerships

If you come across a role that intrigues you but doesnt 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.

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 employees 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 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.

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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 . Visit 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.

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