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

Bristol Myers Squibb

Confirmed live yesterday High trust
Hybrid

Quick summary

Work type
Hybrid
Location
Cambridge, MASan Diego, CABrisbane, CAPrinceton, NJ
Salary
$252,640–$306,137 / yr
Posted
30 days ago
Freshness
Confirmed live yesterday
Closes
Sep 26, 2026

Market check

Salary context

Above market

How this pay compares to similar roles

Similar $237k
This role $279k
$167k most similar roles pay here $321k

This role pays more than 76% of similar roles. Most pay $195,000–$279,093 — the shaded band above. At the midpoint, this role pays about $279k versus about $237k 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 33 open roles on FindRole.

Listed pay typically runs $125,480–$152,049 across 33 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 & Technology

Senior Director, Clinical Pharmacology & Pharmacometrics, Research Business Insights & Technology serves as a strategic leader within the Research Business Insights & Technology team to oversee the clinical pharmacology and pharmacometrics (CPP) technology stack. This role is responsible for building and managing modeling environments, workflow automation, and governed operational capabilities that support the entire lifecycle from preclinical-to-clinical bridging through dose selection and regulatory submission outputs. The successful candidate will manage a team of scientific technologists and engineers to develop tools for population PK, PBPK, QSP, and exposure-response analysis. Key technical requirements include experience with Quarto-based reporting automation, AI/ML applications, and advanced analytics to improve reproducibility and traceability. This role solves the challenge of scaling complex quantitative modeling workflows while ensuring that all outputs remain inspection-ready and compliant for regulatory evidence generation in a highly matrixed research environment.

What you'll do

  • Manage the end-to-end technology stack, applications, and workflows for Clinical Pharmacology and Pharmacometrics (CPP).
  • Develop scalable modeling environments and automated reporting tools to support preclinical-to-clinical transitions and dose selection.
  • Ensure all pharmacometric workflows are reproducible, traceable, and compliant with regulatory inspection standards.
  • Lead the automation of high-priority CPP tasks including simulation execution, data review, and knowledge reuse.
  • Partner with R&D stakeholders to integrate CPP workflows into broader scientific and operational capabilities.
  • Oversee the development of tools for generating quantitative evidence for regulatory submissions and clinical pharmacology summaries.
  • Manage a team of scientific technologists, product leaders, and specialized engineers within the domain.

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 expertise in clinical pharmacology and pharmacometrics.
  • Proven experience implementing CPP applications, PBPK and QSP environments, or quantitative workflow automation.
  • Demonstrated experience supporting regulatory submissions and governed workflows in development-facing settings.
  • Experience applying AI/ML or advanced automation to quantitative modeling or regulated scientific workflows (preferred).
  • Director or Senior Director-level leadership experience is a strong differentiator.
  • Experience building and scaling a specialized scientific technology team is a strong differentiator.
  • Experience as a clinical pharmacology or pharmacometrics technology leader in a top-tier pharmaceutical R&D organization (preferred).

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