Principal Clinical Pharmacologist

Principal Scientist, Clinical PharmacologyWe are looking for a Principal Scientist, Clinical Pharmacology in our Pharmacometrics group. The position will report to the Senior Group Director within Clinical Pharmacology in the General Medicine group. This person will represent Clinical Pharmacology on project teams to provide strategic and scientific expertise to support new and on-going GM clinical programs. This individual is expected to provide significant contributions to PMx deliverables for multiple programs to support the strategies for each program. In addition, this person will prospectively contribute to longer-term development strategies executed over the course of multiple non-clinical experiments, clinical studies and PMx analyses. This person conducts or otherwise oversees the development of PMx analysis plans.When & where:Work Location: Tarrytown, NY, Warren, NJ or Cambridge, MAWork model/flexibility: 4 days per week on siteDiscover your role:Develop and maintain comprehensive strategic CP development plans for assigned programs with SGD supervisionProvide CP subject matter expertise and presentations to the Clinical Study Team/ Development Team and Senior Management/Governance meetings with SGD supervisionCollaborate and assist the Pre-clinical PK/PD Team and research teams to characterize preclinical PK/PD for prediction human PK/PD to accelerate clinical studies and achieve business goalsAssist in drafting and finalization of clinical study protocols and study analysis plans as well as draft, finalize, and/or review clinical pharmacology reportsCollaborate with the Medical Writing Team to incorporate PK/PD sections into clinical study reportsProvide CP support of regulatory documents, communications, and presentations (eg, IND, health authority queries, preparation of BLA summary sections, addressing review inquiries) with SGD supervisionRepresent CP at pre-IND, Type C, preBLA, and other health authority meetings with SGD supervisionWork closely with Quantitative Pharmacology to develop quantitative strategies and to deliver analyses and technical reports to support strategic development plansActively publish work in scientific literatureThis role requires:PhD (example Pharmacometrics, Biology, Pharmacology, Engineering), PharmD, MD6+ years of experience in clinical pharmacologyStrong communications skills to actively engage colleagues cross-functionally at all levels of the organizationInnovative and flexible mindset, keen scientific interest and solid science background are required.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.The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits.