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Senior Scientist , DMPK

Job in Montgomery, Montgomery County, Alabama, 36136, USA
Listing for: Dormont Manufacturing Co
Full Time position
Listed on 2026-07-04
Job specializations:
  • Research/Development
    Pharmaceutical Science/ Research, Research Scientist, Regulatory Compliance Specialist, Drug Discovery
Salary/Wage Range or Industry Benchmark: 115000 - 140000 USD Yearly USD 115000.00 140000.00 YEAR
Job Description & How to Apply Below
Position: Senior Scientist I, DMPK

The Position

Arrowhead Pharmaceuticals is seeking an accomplished Senior Scientist, DMPK to play a key role in advancing our growing pipeline of RNAi-based therapeutics. As a senior member of the Drug Metabolism and Pharmacokinetics (DMPK) function, you will partner closely with multidisciplinary teams of chemists, biologists, and translational scientists to shape strategies that enable successful candidate nomination and IND submissions.

In this high-impact role, you will lead the design and execution of preclinical DMPK studies, guide interpretation of complex PK/PD data, oversee internal and external study activities, and ensure delivery of high-quality datasets that meet regulatory expectations. The ideal candidate brings deep technical expertise, strong problem‑solving skills, and the ability to thrive in a fast‑paced, collaborative environment dedicated to scientific excellence and innovative drug development.

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 Win Nonlin.
  • 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.

115, USD

Arrowhead provides competitive salaries and an excellent benefit package.

Candidates must have current, valid authorization to work in the country where this role is located.

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Position Requirements
10+ Years work experience
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