Senior Lead – Quantitative Clinical Pharmacology & Data Science

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About the Team

Our Clients Data & Quantitative Science function consists of over 500 specialists—from clinical pharmacology, biostatistics, outcomes research, epidemiology, data governance, digital strategy, and more—who harness data and digital innovation to accelerate the development of breakthrough therapies. Working across global project teams, they engage novel data sources (including real‑world and digital streams) and apply advanced analytics like AI and automation. Within this framework, the Quantitative Clinical Pharmacology (QCP) subgroup partners with drug development teams from first‑in‑human through lifecycle management. We’re seeking a seasoned leader who will collaborate closely with the pharmacometrics lead and deliver model‑informed drug development (MIDD) strategies across our portfolio.

Your Mission As a Senior Lead in QCP, you will: Lead scientific and strategic efforts for multiple drug development programs, from early phases to post‑marketing, with significant independence. Define dosage strategies, establish causality evidence, and oversee the execution of clinical pharmacology plans in partnership with pharmacometrics, statistics, DMPK, and other key functions. Champion the implementation of MIDD approaches—such as QSP and MBMA—to support internal decisions and regulatory interactions. Represent clinical pharmacology in regulatory discussions and manage summary documentation for submissions. Conduct or oversee PK/PD analyses, interpret complex multi‑source data, and integrate findings into program planning. Ensure compliance with ethical, regulatory, and clinical practice standards. Mentor and develop junior scientists, contributing to scientific infrastructure and best‑practice initiatives. Serve as an ambassador for clinical pharmacology and data science within the organization and externally—through publications, presentations, and participation in scientific consortia. What You Bring A PharmD or PhD with 8+ years (or MS with 12+ years) in quantitative sciences, including experience in clinical pharmacology/PK‑PD. Oncology drug development experience is a plus. Deep technical mastery of early‑ and late‑stage clinical pharmacology, MIDD strategy, drug development processes, and regulatory frameworks (e.g., FDA, EMA, ICH). Proven ability to deliver and influence cross‑functional teams, set and meet strategic goals, and translate complex science into actionable insights. Strong communication and leadership skills with a collaborative mindset, capable of building alliances across data science, clinical operations, regulatory affairs, and other functions. Excellent judgment, business awareness beyond the immediate discipline, and a track record of advancing scientific strategy in team settings.

Work Model This role is designed as a hybrid position (combining onsite and remote work according to company policy).

U.S. Base Salary Range: $174,500.00 - $274,230.00

Please note: This job posting is just a preview of the full scope of the position. A comprehensive job description is shared by a member of our team.