Senior Director, CPP Technology & Modeling Leadership

Bristol Myers Squibb; Cambridge (MA); On-site; USD 230,000 - 310,000; Full time

Benefits offered by this job

Health Coverage

Wellbeing programs

401(k) plan

Job summary

Bristol Myers Squibb is seeking a strategic, scientifically grounded Senior Director for Clinical Pharmacology & Pharmacometrics to lead CPP applications, modeling environments, and workflow automation across preclinical-to-clinical translation. You will partner with CPP stakeholders to deliver scalable, governed technical capabilities and regulatory‑ready outputs.

The role reports to the VP of Research Business Insights & Technology and requires building a high‑performing, matrixed team while

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.
• Experience supporting regulatory submissions, quantitative reporting, and governed workflows in Development-facing settings.

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 intersects 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.

Skills

Ph.D. in Pharmacometrics

Clinical pharmacology

Pharmacometric applications

Regulatory submissions

Leadership experience

Education

Ph.D. in Pharmaceuticals or related field

Tools

PBPK modelling

QSP platforms

Job description

Bristol Myers Squibb is seeking a strategic, scientifically grounded Senior Director for Clinical Pharmacology & Pharmacometrics to lead CPP applications, modeling environments, and workflow automation across preclinical-to-clinical translation. You will partner with CPP stakeholders to deliver scalable, governed technical capabilities and regulatory‑ready outputs.

The role reports to the VP of Research Business Insights & Technology and requires building a high‑performing, matrixed team while