Jobs · Analyst · Wisconsin

Senior Scientist I, DMPK

CHEManager International · Madison, WI · Yesterday
Analyst$115k–$140k/yrFull-time

Responsibilities

  • Develop and implement in vitro and in vivo DMPK strategies to support preclinical development for compounds across multiple indications and routes of administration.
  • Manage all DMPK activities, including oversight of internal resources and CRO partners to ensure high-quality and timely data delivery.
  • Design, supervise, and execute preclinical PK studies, including non-compartmental analysis (NCA), data interpretation, reporting, and communication of PK/PD insights to project teams.
  • Prepare and deliver IND-enabling DMPK packages, ensuring compliance with regulatory expectations and contributing to regulatory submissions.
  • Apply working knowledge of GLP/GCP principles and ensure appropriate documentation for regulated studies.
  • Support GLP toxicokinetic (TK) study design, analysis, and reporting.
  • Oversee metabolite identification in preclinical and clinical samples using high-resolution mass spectrometry (HRMS).
  • Contribute to a dynamic, fast-paced DMPK team by offering scientific leadership, troubleshooting support, and cross-functional collaboration.
  • Maintain a current understanding of clinical pharmacology literature and regulatory guidance for oligonucleotide/RNAi therapeutics.

Requirements

  • PhD in Pharmacometrics, Drug Metabolism, Pharmaceutical Sciences, or a related discipline with at least 3 years of industry experience.
  • Deep and broad expertise in DMPK, with working knowledge of nucleotide or oligonucleotide drug metabolism and distribution highly desired.
  • Hands-on experience with in vitro ADME assays, in vivo PK studies, drug-drug interaction (DDI) evaluations, and Phoenix WinNonlin.
  • Experience with LC-MS/MS and HRMS, ideally applied to oligonucleotide therapeutics.
  • Strong background in organic chemistry, biochemistry, and drug biotransformation.
  • Demonstrated experience in drug development and understanding of regulatory processes.
  • Excellent interpersonal, verbal, and written communication skills, with the ability to interpret and present complex scientific data clearly.

Qualifications

  • Current, valid authorization to work in the country where this role is located.

Benefits

Arrowhead provides competitive salaries and an excellent benefit package.

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