Principal Clinical Pharmacologist

Regeneron Pharmaceuticals

7d•$150,500 - $245,500•Hybrid

About The Position

We are looking for a Principal Scientist, Clinical Pharmacology in our Pharmacometrics (PMx) group. The position will report to the Senior Group Director (SGD) within Clinical Pharmacology (CP) in the General Medicine (GM) 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.

Requirements

PhD (example Pharmacometrics, Biology, Pharmacology, Engineering), PharmD, MD
6+ years of experience in clinical pharmacology
Strong communications skills to actively engage colleagues cross-functionally at all levels of the organization
Innovative and flexible mindset, keen scientific interest and solid science background are required.

Responsibilities

Develop and maintain comprehensive strategic CP development plans for assigned programs with SGD supervision
Provide CP subject matter expertise and presentations to the Clinical Study Team/ Development Team and Senior Management/Governance meetings with SGD supervision
Collaborate 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 goals
Assist in drafting and finalization of clinical study protocols and study analysis plans as well as draft, finalize, and/or review clinical pharmacology reports
Collaborate with the Medical Writing Team to incorporate PK/PD sections into clinical study reports
Provide CP support of regulatory documents, communications, and presentations (eg, IND, health authority queries, preparation of BLA summary sections, addressing review inquiries) with SGD supervision
Represent CP at pre-IND, Type C, preBLA, and other health authority meetings with SGD supervision
Work closely with Quantitative Pharmacology to develop quantitative strategies and to deliver analyses and technical reports to support strategic development plans
Actively publish work in scientific literature