Senior Dir, Clinical Pharmacology & Pharmacometrics

Bristol Myers Squibb

Quick summary

Work type
On-site
Location
Cambridge Crossing, MA · San Diego, CA · Brisbane, CA · Princeton, NJ
Salary
$252,640–$306,137 / yr
Posted
3 days ago
Closes
Sep 30, 2026

Market check

Salary context

Above market

How this pay compares to similar roles

Similar $177k
This role $279k
$102k most similar roles pay here $328k

This role pays more than 94% of similar roles. Most pay $139,425–$214,500 — the shaded band above. At the midpoint, this role pays about $279k versus about $177k 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 32 open roles on FindRole.

Listed pay typically runs $135,320–$163,976 across 32 roles with salary data.

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View all roles at Bristol Myers Squibb

At a glance

TL;DR · Senior Dir, Clinical Pharmacology & Pharmacometrics

Bristol Myers Squibb is hiring a Senior Director for Clinical Pharmacology & Pharmacometrics to lead the development and scaling of technology solutions that support quantitative preclinical-to-clinical bridging through clinical PK/PD, dose selection, and regulatory evidence generation. This role involves partnering with scientific teams to deliver applications, modeling environments, and workflow automation, ensuring operational excellence and continuous improvement across CPP use cases. The ideal candidate will have a Ph.D. in a relevant field, extensive experience in pharmaceutical R&D, and expertise in implementing CPP applications and quantitative workflows. They should be proficient in AI/ML for regulated scientific workflows and possess strong leadership skills to build and scale a specialized team within a matrixed organization. This position is crucial as the company reimagines how technology enables decision-making across its Research and Development pipeline.

What you'll do

  • Lead the integration of clinical pharmacology and pharmacometrics workflows with scientific, data, and operational capabilities.
  • Ensure reliability, governance, and continuous improvement across modeling environments and reporting workflows for CPP use cases.
  • Automate priority CPP workflows to enhance efficiency in model execution, simulation, traceability, review, and evidence reuse.
  • Support regulatory submissions through robust tooling, reproducible workflows, and inspection-ready practices for quantitative deliverables.
  • Develop a durable technology foundation that scales with pipeline demand and integrates across the broader R&D ecosystem.

What we're looking for

  • Ph.D. in a quantitative field such as pharmacometrics or clinical pharmacology.
  • 12+ years of experience in pharmaceutical R&D with expertise in clinical pharmacology and pharmacometrics.
  • Proven track record implementing CPP applications, PBPK/QSP environments, and clinical PK/PD systems.
  • Experience supporting regulatory submissions through robust reporting and governed workflows.
  • Leadership in building and scaling specialized scientific technology teams within a matrixed organization.

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