Senior Director, Clinical Pharmacology & Pharmacometrics, Research Business Insights & Technology
Bristol Myers Squibb
August 13, 2026
Remote friendly (Cambridge, MA)
United States
Clinical Research and Development
Role Overview
Senior Director, Clinical Pharmacology & Pharmacometrics (CPP). Partner with Clinical Pharmacology, Pharmacometrics, Quantitative Pharmacology, and Translational Medicine stakeholders to deliver end-to-end CPP applications, modeling environments, workflow automation, and governed operational capabilities (preclinical-to-clinical bridging through clinical PK/PD, dose/regimen decisions, and submission-support outputs).
Mission & Impact
- Provide scalable CPP application/workflow backbone across translation, clinical PK/PD, dose selection, exposure-response, and model-informed decisions.
- Improve speed, quality, reproducibility, traceability, and inspection-readiness of CPP workflows.
- Strengthen regulatory submissions via robust, reusable, auditable quantitative reporting/evidence.
- Enable governed automation (reporting, simulation, execution, review, knowledge reuse) and scale with pipeline demand.
Sub-Areas in Scope
Population PK/PK-PD/exposure-response/dose optimization; PBPK/QSP/DDI modeling; clinical PK/PD systems and operational tooling; CPAR and reporting automation (e.g., Quarto); translational workflows; workflow governance/audit trails/validation/access controls for regulated environments; AI-enabled analytics.
Key Responsibilities
- Single BI&T point of accountability for CPP technology/workflows/support end to end.
- Own CPP applications, modeling environments, reporting workflows, and operational support.
- Lead automation; ensure reliability, governance, continuous improvement; support inspection-ready regulatory deliverables.
- Partner on translational/lab/diagnostic/bioanalytical intersections and with R&D Data on data-product strategy.
- Lead and grow specialized scientific technologists, product leaders, and engineers.
Required Qualifications
- Ph.D. in Pharmacometrics/Clinical Pharmacology/Pharmaceutical Sciences/Biostatistics or related.
- 12+ years in pharma R&D with deep CPP/model-informed drug development experience.
- Proven experience implementing/leading CPP applications, PBPK/QSP, clinical PK/PD systems, and/or quantitative workflow automation.
- Experience supporting regulatory submissions and governed quantitative reporting in Development-facing settings.
Preferred Qualifications
- Experience applying AI/ML or advanced automation to quantitative modeling/reporting/regulatory workflows.
- Director/Senior Director leadership experience; experience building/scaling a specialized scientific technology team.
Benefits (explicitly stated)
- Health coverage (medical, pharmacy, dental, vision).
- Wellbeing support programs (e.g., EAP).
- Financial well-being/protection (401(k), disability, life insurance, etc.).
- Paid time off (flexible time off for US Exempt roles; vacation/holidays for other groups).
Senior Director, Clinical Pharmacology & Pharmacometrics (CPP). Partner with Clinical Pharmacology, Pharmacometrics, Quantitative Pharmacology, and Translational Medicine stakeholders to deliver end-to-end CPP applications, modeling environments, workflow automation, and governed operational capabilities (preclinical-to-clinical bridging through clinical PK/PD, dose/regimen decisions, and submission-support outputs).
Mission & Impact
- Provide scalable CPP application/workflow backbone across translation, clinical PK/PD, dose selection, exposure-response, and model-informed decisions.
- Improve speed, quality, reproducibility, traceability, and inspection-readiness of CPP workflows.
- Strengthen regulatory submissions via robust, reusable, auditable quantitative reporting/evidence.
- Enable governed automation (reporting, simulation, execution, review, knowledge reuse) and scale with pipeline demand.
Sub-Areas in Scope
Population PK/PK-PD/exposure-response/dose optimization; PBPK/QSP/DDI modeling; clinical PK/PD systems and operational tooling; CPAR and reporting automation (e.g., Quarto); translational workflows; workflow governance/audit trails/validation/access controls for regulated environments; AI-enabled analytics.
Key Responsibilities
- Single BI&T point of accountability for CPP technology/workflows/support end to end.
- Own CPP applications, modeling environments, reporting workflows, and operational support.
- Lead automation; ensure reliability, governance, continuous improvement; support inspection-ready regulatory deliverables.
- Partner on translational/lab/diagnostic/bioanalytical intersections and with R&D Data on data-product strategy.
- Lead and grow specialized scientific technologists, product leaders, and engineers.
Required Qualifications
- Ph.D. in Pharmacometrics/Clinical Pharmacology/Pharmaceutical Sciences/Biostatistics or related.
- 12+ years in pharma R&D with deep CPP/model-informed drug development experience.
- Proven experience implementing/leading CPP applications, PBPK/QSP, clinical PK/PD systems, and/or quantitative workflow automation.
- Experience supporting regulatory submissions and governed quantitative reporting in Development-facing settings.
Preferred Qualifications
- Experience applying AI/ML or advanced automation to quantitative modeling/reporting/regulatory workflows.
- Director/Senior Director leadership experience; experience building/scaling a specialized scientific technology team.
Benefits (explicitly stated)
- Health coverage (medical, pharmacy, dental, vision).
- Wellbeing support programs (e.g., EAP).
- Financial well-being/protection (401(k), disability, life insurance, etc.).
- Paid time off (flexible time off for US Exempt roles; vacation/holidays for other groups).