Senior Quantitative Pharmacologist

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About the role

Build Our Future Together As a Senior Quantitative Pharmacologist this individual is expected to provide significant contributions to Pharmacometrics deliverables in support of multiple programs while also developing an ability to understand the strategic positioning for these programs in Pharmacometrics as well as across the organization. Through the application of state-of-the-art knowledge in pharmacokinetics and pharmacodynamics; is responsible for the execution of PK, PD, and other types of quantitative analyses that significantly contribute to the development of multiple programs. When & where: • Work Location: Tarrytown, NY, Warren, NJ, Cambridge, MA • Work model/flexibility: 4 days per week onsite or remote Discover your role: • Collaborate across functions to plan, design, implement, and analyze pharmacometrics (PMx) studies supporting drug development programs. • Apply standardized scientific approaches to evaluate and interpret in vitro and in vivo pharmacokinetic (PK), pharmacodynamic (PD), and PK/PD data. • Conduct a broad range of quantitative analyses including NCA, compartmental modeling, population PK, exposure-response, translational, and disease modeling. • Interpret study results and develop scientifically sound conclusions and recommendations to support development decisions. • Prepare accurate, timely, and well-articulated study reports, technical summaries, and regulatory submission documents. • Partner with PMx Research Specialists, programmers, statisticians, and scientific writers to develop tables, figures, listings (TFLs), and supporting analyses for internal and regulatory deliverables. • Contribute PMx expertise to Research and Global Clinical Study Team (GCST) meetings, including input on study design, analysis strategy, and interpretation of results. • Support regulatory interactions by preparing analyses and background materials for agency meetings, including pre-IND, End-of-Phase 2, and pre-BLA submissions. • Monitor project timelines, deliverables, and completion of assigned tasks; may serve as the PMx representative on cross-functional development teams with appropriate guidance. • Maintain compliance with PMx operating procedures, quality standards, and the company's code of ethical conduct. This role requires: • PhD in Quantitative Pharmacology, Pharmacometrics, Engineering, or a related field with 3+ years of experience • Demonstrated expertise in population PK/PD, exposure–response, or mechanistic modeling (systems biology, or QSP) using tools such as NONMEM, Monolix, Simulx, MATLAB/Simbiology and R. • Hands-on experience with a broad range of quantitative and computational tools and a strong publication record. • Exceptional communication and interpersonal skills, with the ability to influence and partner effectively across technical and non-technical teams. Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all  qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impo

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