Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
MS
Merck Sharp Dohme
Senior Director, Quantitative Systems Pharmacology - Oncology (Hybrid or Remote)
Career Insights for Pharmacology Research Scientist
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Arkansas data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Pharmacology Research Scientist performs scientific research with the aim of discovering new solutions or improving existing ones within the field of use and effects of drugs.
$161,666 / year median in Arkansas
+6% projected growth
Job Description
Senior Director, Quantitative Systems Pharmacology - Oncology (Hybrid or Remote)
at Merck in Little Rock, Arkansas, United States
Job Description
Job Description
We are seeking an accomplished scientific leader to join the Quantitative Pharmacology and Pharmacometrics -Oncology (QP2 Oncology) team as Senior Director, Quantitative Systems Pharmacology (QSP). QP2 Oncology is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical pharmacology, mechanistic PK-PD modeling and pharmacometrics of oncology drugs from post-preclinical candidate (PCC) selection through registration.
Our Senior Directors are recognized experts in quantitative drug development and possess a deep, integrated understanding of both the science and the strategic, end-to-end dimensions of oncology drug development. Reporting directly to Executive Director and Section Head, QP2 Oncology, the Senior Director will provide leadership and scientific oversight to all QSP and mechanistic modeling efforts across the oncology portfolio.
Primary Responsibilities
+ Lead and shape the QSP strategy across the oncology portfolio, ensuring alignment with program goals and organizational priorities.
+ Lead, mentor, and develop a team of quantitative scientists in a matrixed role.
+ Work in close collaboration with QP2 Oncology team, preclinical DMPK and modeling teams, biologists, clinicians, and other line functions to utilize mechanistic/ QSP modeling for dose selection, combination strategies and clinical trial design.
+ Ensure high-quality, regulatory grade QSP deliverables for internal decisions, submissions, and scientific advice meetings.
+ Contribute to regulatory strategy through preparation of QSP reports, briefing documents, and presentations.
+ Foster a culture of scientific rigor, excellence, collaboration, and innovation and develop best practices for QSP modeling.
+ Partner with senior leaders in Translational Modeling, Discovery and Clinical Development to define modeling strategies that influence program design and key decisions.
+ Represent the company at scientific conferences, external collaborations, consortia, and industry working groups.
+ Stay at the forefront of emerging methodologies in QSP and promote innovation.
+ Manage activities related to budget planning, QSP vendor identification and outsourcing of QSP analyses and contract requisitions.
Minimum education required:
+ Ph.D., with at least ten years of pharmaceutical drug development experience relating to: systems pharmacology, systems biology, PKPD, mathematics, chemical/biomedical engineering or related field.
+ Masters or PharmD, with at least fifteen years of experience, where "experience" means having a record of increasing responsibility and independence in a similar role in pharmaceutical drug development.