Associate Director, Quantitative Pharmacology

🕒 Maio 31

🗽 New York – Remoto

🗽 New York – Remote

💵 $176.100 - $287.300 / ano

⏰ Tempo Integral

🟠 Sênior

👔 Diretor

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Regeneron

SiteLinkedInTodas as Vagas

10.000+ funcionários

Fundada em 1988

🧬 Biotecnologia

💊 Farmacêutico

⚕️ Seguro de Saúde

💰 Post-IPO Equity em 2023-10

Biotechnology • Pharmaceuticals • Healthcare Insurance

A Regeneron é uma empresa de biotecnologia dedicada a transformar descobertas científicas em medicamentos que mudam vidas. A empresa se concentra em uma variedade de doenças graves, incluindo doenças alérgicas, cardiovasculares e metabólicas, neurociência, oncologia, hematologia, oftalmologia e doenças raras. Isso é alcançado integrando biologia e tecnologia para desenvolver biológicos inovadores e medicamentos genéticos. A Regeneron está comprometida com a equidade em saúde, sustentabilidade ambiental e apoio ao talento futuro em STEM por meio de iniciativas como o Regeneron Science Talent Search. Mantendo altos padrões éticos e responsabilidade corporativa, a Regeneron visa ultrapassar os limites da ciência para melhores soluções de saúde.

Descrição

• Leading model-informed drug development strategies supporting one or more therapeutic areas across modalities including antibodies, siRNA, and gene therapies. • Driving model-informed development (MIDD) and pharmacometrics strategies in partnership with Clinical Pharmacology, Biostatistics, Clinical and Translational teams to support regulatory and clinical decision-making. • Leading the QP evaluation of one or more assets, accountable for timely delivery of population PK/PD, exposure–response, and translational modeling analyses. • Representing QP at program and governance meetings, communicating quantitative insights clearly to non-modeling audiences. • Contributing to regulatory interactions and authoring key components of regulatory documents related to QP (e.g., IB, briefing books, etc.). • Mentoring and developing junior scientists and fostering a culture of scientific rigor and collaboration. • Identifying and implementing process improvements, new modeling approaches, and innovative quantitative tools to enhance efficiency and impact. • Ensuring analyses and documentation are of the highest scientific quality and regulatory compliance.

🎯 Requisitos

• PhD in Quantitative Pharmacology, Pharmacometrics, Engineering, or a related field with 6+ years of post-doctoral or industry experience; or MS with 9+ years of relevant experience. • Demonstrated expertise in population PK/PD, exposure–response, or mechanistic modeling (systems biology, or QSP) using tools such as NONMEM, Monolix, Simulx, MATLAB/Simbiology and R. • Proven track record of delivering analyses supporting regulatory submissions and engaging directly with agencies (e.g., FDA, EMA, PMDA). • Hands-on experience with a broad range of quantitative and computational tools and a strong publication record.

🏖️ Benefícios

• health and wellness programs (including medical, dental, vision, life, and disability insurance) • fitness centers • 401(k) company match • family support benefits • equity awards • annual bonuses • paid time off • paid leaves (e.g., military and parental leave)