We are looking for a highly motivated 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. You will represent CP on project teams to provide strategic and scientific expertise to support new and ongoing 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. You will conduct or otherwise oversees the development of PMx analysis plans.
This role must be onsite a minimum of 3-days per week at either our Tarrytown, NY or Basking Ridge, NJ location.
A typical day as a Clinical Pharmacologist looks like::
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
Draft, finalize, and/or review CP 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
This role may be for you if:
Have 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
Have a passion for science
In order to be considered qualified for this role, A PhD, Biology, Pharmacology, Engineering, Pharmacy (Pharm.D.), Medicine (MD) and at least 4 years of relevant Clinical Pharmacology experience. Oncology experience is strongly preferred, but not required.
#MDJobs
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
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, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
Salary Range (annually)
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