Regeneron

Healthcare

DirectorGroupQuantitativePharmacology

$205–342k Tarrytown, New York, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Director candidates.

The Brief

“Director Group Quantitative Pharmacology at Regeneron. Skills: Quantitative Pharmacology, Pharmacometrics, Drug development. Manage PK/PD evaluation. Deliver quantitative analyses”

Industry & Context.

Healthcare
Problems you'll solve

Complex problem solving

What They're Looking For.

Must Have

PhD, 10+ years experience, Degree in Quantitative Pharmacology, Hands on usage of quantitative tools, Publication record in the field, Excellent interpersonal skills, Excellent communication skills, Ability to communicate complex information succinctly, Proven experience developing QP elements of regulatory strategy, Proven experience interacting with regulatory agencies without supervision

Nice to Have

PhD preferred, Specific ML framework experience, Cloud platform certs

What You'll Do.

Manage PK/PD evaluation

Deliver quantitative analyses

Interpret quantitative analyses

Message quantitative analyses to management

Deliver reports for review

Inform management of developments

Ensure analyses quality

Ensure analyses accuracy

Develop meaningful story-lines for reports

Ensure reports have appropriate messaging

Ensure documents have functional review

Ensure documents are suitable for senior management review

Solve complex problems

Identify solutions broadly

Publish work in scientific literature

Contribute to multi-disciplinary meetings

How You'll Work.

Team & Collaboration

Multi-disciplinary meetings

Communication Scope

Written communication; Oral communication; Succinct communication

Full Job Description

As a Director in Pharmacometrics (Quantitative Pharmacology), this individual is accountable for the delivery of support for one or more research & development programs, within their pharmacometrics discipline. In this capacity the Director is accountable for the timely and accurate delivery of needed quantitative analyses, interpretation, and messaging to PMx management, as well as the timely delivery of well-constructed and well-messaged reports for PMx review. **A day in the life of a Director may look like:** * Manages and is accountable for the PK/PD evaluation of a small portfolio of products or projects. * Works independently, with guidance in only the most complex situations. * Informs PMx management of important program and regulatory developments in a timely manner. * Ensures analyses and documentation are of the highest quality and accuracy. * Ensures that reports and other documents have the appropriate messaging and that a meaningful “story-line” is developed. * Ensures that study reports and other documents have an appropriate functional review and are suitable for review by senior management. * Solves complex problems; takes a broad perspective to identify solutions. * Has a strong publication record and actively publishes work in scientific literature * Makes contributions to multi-disciplinary meetings by sharing cross-functional skills and knowledge. * Has excellent interpersonal and communication skills, both written and oral, and has ability to communicate complex information succinctly. **This may be the right role for you if you:** * Are fully knowledgeable of pharmacokinetic /pharmacodynamic principles, pharmacology, biology, and quantitative aspects of drug development as well as having an advanced knowledge of pharmaceutical drug development. * Possess a deep understanding of scientific literature and technical skills in a number of PK/PD methods and techniques. Has extensive knowledge base of the work in overall scientific community in own

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