Senior Clinical Pharmacologist

We are looking for a Senior Clinical Pharmacologist. This individual will plan, design, implement and analyze pharmacokinetic & pharmacodynamic studies, working with colleagues in Clinical Pharmacology, Quantitative Pharmacology, Preclinical PK-PD, Toxicology, Bioanalytical, Therapeutic Focus Areas and Clinical Development / Regulatory Affairs.

We expect the person in this role to contribute to the scientific understanding of human PK/PD for the assigned project(s), based on quantitative evaluations of the pharmacokinetic and pharmacodynamic profile.

A day in the life of a Clinical Pharmacologist may look like:

-  Planning, designing, implementing, and analyzing routine PMx studies to advance scientific knowledge, in collaboration with other team members.

-  Performing analyses such as NCA, compartmental modeling, translational modeling, E-R analyses.

-  Working to prepare TFLs to support IND/CTA, PK WSs, Tox WS, Pharm WS, CSRs, DSURs, IB and other documents. Collaborates with Scientific Writing (and where appropriate with PMx Stats Programming team) to ensure TFLs for PMx reports are complete.

-  With close supervision from senior PMx staff, supporting preparation of material to be used in regulatory interactions. Preparation of PMx materials for regulatory background packages, e.g. for pre-IND, EOP2, and pre-BLA meetings is also in scope. Performs additional analyses as required to support regulatory interactions.

-  Working in conjunction with Scientific Writing, QC and QAA (as required) to issue study reports in support of IND/CTA submissions and other regulatory documents.

-  Actively publishing work in scientific literature

This may be the right role for you if:

-  You want to participate in technical working groups, providing support for process improvement initiatives.

-  You enjoy working in cross-functional teams with forward-thinking, passionate, driven teammates

 In Order to be Considered for this role, you must have:

A minimum of a PhD/PharmD and 3 + years of proven ability with PMx concepts and techniques, post-degree. We expect this experience to include advanced pharmacokinetics, advanced pharmacological principles, non-compartmental analysis methods. Familiarity with other methodologies such as exposure-Response analysis methods, translational modeling/pharmacology, nonlinear Mixed Effects modeling, logistic regression, survival analysis, Bayesian approaches, disease modeling/QSP is also advantageous.

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Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits including health and wellness programs, fitness centers and 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. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.

The salary ranges provided are shown in accordance with U.S. law and apply to U.S. based positions, where the hired candidate will be located in the U.S. If you are outside the U.S, please speak with your recruiter about salaries and benefits in your location.

Salary Range (annually)

$114,900.00 - $187,500.00