About this opportunity
Regeneron Pharmaceuticals, Inc. lists this Pharmacokineticist, PPK/PD opportunity in village of tarrytown, New York. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Build Our Future Together
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Pharmacokineticist for PPK/PD to serve as a senior independent contributor in the Translational Pharmacokinetics and Pharmacodynamics (TPK/PD) Group, taking ownership of PK/PD analyses end-to-end and serving as a pharmacokinetics point of contact across assigned studies. This person will independently plan and execute non-compartmental and compartmental PK/PD analyses in support of nonclinical and (potentially) clinical studies using Phoenix WinNonlin and other analysis software, and will prepare and quality‑control standardized datasets from CRO and internal bioanalytical data for regulatory submission. This person will lead PK/TK protocol design/input, support CRO studies, produce Pharmacometrics deliverables and regulatory tables/figures/listings, contribute to standard‑setting and best practices for the group, and mentor and provide technical guidance to junior analysts, following all SOPs to ensure GxP/GLP compliance.
When & Where:
This role will sit at our Tarrytown, NY office and is expected to be on‑site 4 days per week.
Discover Your Role:
Independently leads, performs, and takes ownership of non‑compartmental PK and compartmental PK/PD analyses in support of nonclinical and (potentially) clinical studies, according to GxP as appropriate, and serves as the pharmacokinetics point of contact and lead analyst for assigned studies.
Conducts compliance‑related activities (SOPs, etc.); ensures regulatory‑submission conformance, data integrity, and GxP compliance; adheres to controlled SOPs; helps set group standards by authoring/revising SOPs and providing senior compliance review of others' deliverables; and meets mandatory‑training and data‑confidentiality requirements.
Owns the preparation, quality control, and senior review of standardized CDISC SEND datasets (e.g., PC/PP domains and associated SUPPQUAL) from CRO and internal bioanalytical data, with auditable, source‑traceable derivations that conform to controlled terminology and regulatory‑submission standards, and sets and maintains the dataset standards and conventions the group follows.
Owns and leads CRO study support; tracks study requirements, project priorities, status, and milestones; serves as the primary PK point of contact and liaison to CROs and functional groups; and drives coordination across the study lifecycle.
Independently owns and executes a broad array of work supporting department priorities in routine and non‑routine Pharmacometrics deliverables on study design, analysis, and reporting, and sets methodology and best‑practice standards for the group.
Produces and formats tables and listings (TFLs), including PK concentration and parameter summaries, for regulatory documents using validated tools (e.g., Phoenix WinNonlin, R), and owns, sets, and reviews against the group's consistent, submission‑ready presentation standard.
Produces and reviews figures and graphical outputs (e.g., concentration‑time profiles) for study reports and regulatory submissions using validated tools, and owns and sets the group's graphical presentation standard.
This Role Requires:
Bachelors degree with 5-7 years of professional experience, or a Masters degree with 3-5 years of professional experience
Strong, in‑depth understanding of pharmacokinetics concepts and techniques
Proficient in relevant software, including Phoenix WinNonlin; knowledge of NLME/population PK a plus
Experience in animal PK/TK studies, including protocol design & study conduct
Able to clearly describe and perform advanced pharmacometric techniques, interpret results independently, and mentor and provide technical guidance to junior staff
Ability to help set group standards and best practices, with experience working in a GLP environment and following SOPs
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 impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.