Director Quantitative Pharmacology

Regeneron is seeking a Director to join our Pharmacometrics team!

In this role, a typical day might include:

As a Director in Pharmacometrics (Quantitative Pharmacology), this individual is 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.

This role might be for you if can:

• 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. \

• Has strong collaborative skills and is effective at building alliances across functions.

• Excellent interpersonal and communication skills both written and oral and ability to communicate complex information succinctly.

• Strong collaborative skills and effective at building alliances across functions.

• Ability to effectively influence colleagues and multi-disciplinary project teams.

• Able to handle all types of projects and leverage higher level staff for technical input and brainstorming to implement solutions for complex projects. Able to work with considerable ambiguity.

• Identifies business problems and works in team to craft solutions. Able to interact with regulatory agencies without supervision, and with company to develop regulatory strategy.

• Active professionally and finds ways to represent company externally.

To be considered for this opportunity, you must have the following: ​

• Is 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.

• Possesses 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 discipline.

• Is recognized as an expert in own area within the organization.

• Has extensive regulatory experience through authoring of regulatory briefing books, CTD summaries, contribution at HA meetings, HA negotiations through regulatory reviews and approvals of BLA or equivalent.

• Decisions are guided by policies, procedures and business plan; receives guidance from head of function.

• PhD with 8+ years of relevant experience

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,