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

Bristol Myers Squibb

Confirmed live today High trust
Hybrid

Quick summary

Work type
Hybrid
Location
Cambridge Crossing, MASan Diego, CABrisbane, CAPrinceton, NJ
Salary
$252,640–$306,137 / yr
Employment
Full-time
Posted
40 days ago
Freshness
Confirmed live today
Closes
Dec 5, 2026

Market check

Salary context

Above market

How this pay compares to similar roles

Similar $238k
This role $279k
$159k $322k
below market most similar roles pay here above market

This role pays more than 75% of similar roles. Most pay $187,665–$287,681 — the blue band above. At the midpoint, this role pays about $279k versus about $238k for comparable roles.

Based on 240 similar postings.

Employer

About Bristol Myers Squibb

Bristol Myers Squibb is a global biopharmaceutical company committed to discovering, developing and delivering innovative medicines to patients.

Bristol Myers Squibb currently has 34 open roles on FindRole.

Listed pay typically runs $153,830–$186,404 across 26 roles with salary data.

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View all roles at Bristol Myers Squibb

At a glance

TL;DR · Senior Director, Clinical Pharmacology & Pharmacometrics, Research Business Insights/Information Technology

JOB TITLE: Senior Director (QSP), Clinical Pharmacology & Pharmacometrics, Research Business Insights/Information Technology The Senior Director (QSP), Clinical Pharmacology & Pharmacometrics, Research Business Insights/Information Technology leads a team of scientific technologists, product leaders, and specialized engineers. This leader serves as the primary point of accountability for the Clinical Pharmacology and Pharmacometrics technology stack, providing a scalable application and workflow backbone for Research and Development. Key responsibilities include delivering modeling environments, workflow automation, and governed operational capabilities to support quantitative preclinical-to-clinical bridging, dose selection, and regulatory evidence generation. The role requires expertise in population PK, PK/PD, PBPK, and QSP modeling. Candidates must utilize Quarto-based reporting automation, AI-enabled analytics, and advanced automation to improve reproducibility and inspection-readiness. This position solves the technical challenge of scaling complex quantitative pharmacology workflows while ensuring audit trails and data integrity for regulatory submissions.

What you'll do

  • Serve as the primary point of accountability for Clinical Pharmacology and Pharmacometrics (CPP) technology, applications, and workflows.
  • Own the modeling environments, reporting workflows, and operational support for core CPP use cases.
  • Lead the automation of priority CPP workflows, including model execution, simulation, and evidence reuse.
  • Ensure operational excellence, reliability, and governance across clinical PK/PD systems and reporting applications.
  • Support quantitative regulatory deliverables through the development of reproducible workflows and inspection-ready practices.
  • Partner with R&D data and lab teams to integrate CPP workflows with broader scientific and operational capabilities.
  • Lead and grow a specialized team of scientific technologists, product leaders, and engineers.

What we're looking for

  • Ph.D. in Pharmacometrics, Clinical Pharmacology, Pharmaceutical Sciences, Biostatistics, or a related quantitative field.
  • 12+ years of experience 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.
  • Director or Senior Director-level leadership experience; experience building and scaling a specialized scientific technology team is a strong differentiator.
  • Experience applying AI/ML or advanced automation to quantitative modeling, reporting, or regulated scientific workflows is preferred.
  • Experience as a clinical pharmacology or pharmacometrics technology leader inside a top-tier pharmaceutical R&D organization (preferred).
  • Track record of platforms that improved dose selection, quantitative decision-making, or regulatory execution in Development-facing settings (preferred).

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