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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Associate Director - Preclinical and Translational PK/PD

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-timeTarrytown, NY, USA$176.1k - $287.3k /yr

About the Job

Requirements

  • A PhD in Pharmacology, Pharmacokinetics, Biology/Molecular Biology, or Biochemistry is required, along with more than 8 to 10 years of relevant experience in biotech or pharma.
  • A deep theoretical and applied understanding of pharmacokinetics and pharmacodynamics is required to interpret the pharmacology and biology of therapeutic proteins.
  • Experience planning, coordinating, and leading pharmacokinetics and/or pharmacokinetics/pharmacodynamics studies and analyzing related data is required.
  • Familiarity with pharmacokinetics/pharmacodynamics software such as WinNonlin, data visualization software, and artificial intelligence software is required, along with experience writing scientific reports and regulatory summaries.

Responsibilities

  • Provide input and oversight for preclinical in vivo studies and coordinate with and influence scientific teams conducting these studies.
  • Manage nonclinical pharmacokinetics studies.
  • Analyze and present pharmacokinetics/pharmacodynamics data to project teams and senior management.
  • Prepare summary reports for regulatory submissions.
  • Serve as a subject matter expert on preclinical pharmacokinetics/pharmacodynamics within Discovery-stage project teams and guide the design of preclinical pharmacokinetics/pharmacology studies.
  • Collaborate with Therapeutic Proteins, Therapeutic Function Areas, Assay Development, Precision Medicine, Preclinical Operations, and pharmacokinetics/pharmacodynamics management to develop and execute project pharmacokinetics strategies.
  • Communicate project team queries, expectations, and timelines to management.
  • Conduct and report pharmacokinetics/pharmacodynamics analyses based on preclinical study data.
  • Work with Toxicology, Pathology, Clinical Pharmacology, and Quantitative Pharmacology teams in the Drug Safety and Pharmacometrics department to deliver data and regulatory documents supporting project progression.
  • Maintain current knowledge of scientific literature, regulatory guidance, and best practices related to pharmacokinetics/pharmacodynamics.

Desired Qualifications

  • Experience with modalities such as small interfering RNA (siRNA), CRISPR-based therapeutics, and cell therapies is highly beneficial.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

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