Arrowhead Research

Senior Scientist I, DMPK

Arrowhead Research$115K — $140K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD in Pharmacometrics, Drug Metabolism, Pharmaceutical Sciences, or related field with 3+ years of industry experience
  • Expertise in DMPK with emphasis on nucleotide or oligonucleotide drug metabolism
  • Hands-on experience with in vitro ADME assays and in vivo PK studies
  • Familiarity with LC-MS/MS and HRMS, especially for oligonucleotide therapeutics
  • Strong foundation in organic chemistry, biochemistry, and drug biotransformation
  • Demonstrated experience in drug development and regulatory processes
  • Excellent communication skills for presenting complex scientific data

Responsibilities

  • Develop and implement DMPK strategies for preclinical development across multiple indications
  • Manage DMPK activities, including oversight of internal teams and CROs for high-quality data delivery
  • Design and execute preclinical PK studies, including non-compartmental analysis and data interpretation
  • Prepare IND-enabling DMPK packages ensuring regulatory compliance
  • Apply GLP/GCP principles and manage documentation for regulated studies
  • Support design, analysis, and reporting of GLP toxicokinetic studies
  • Oversee metabolite identification in preclinical and clinical samples using HRMS
  • Contribute scientific leadership and facilitate collaboration within the DMPK team

Benefits

  • Competitive salary package
  • Excellent benefits including health and retirement plans
  • Opportunity to work in a fast-paced, science-driven environment
  • Engagement with multidisciplinary teams fostering innovation
  • Professional development opportunities within a growing company
Full Job Description
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 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.


Wisconsin pay range

$115,000-$140,000 USD

Arrowhead provides competitive salaries and an excellent benefit package.

About Arrowhead Research

Arrowhead Research is a biotechnology company that develops RNA interference (RNAi) therapeutics. The company was founded in 2007 and is headquartered in Pasadena, California. Arrowhead's RNAi technology targets specific genes to silence their expression, which can be used to treat a variety of diseases. The company's pipeline includes treatments for liver disease, cancer, and cardiovascular disease. Arrowhead has partnerships with pharmaceutical companies such as Amgen and Janssen Pharmaceuticals. The company has received FDA approval for some of its products and is conducting clinical trials for others.
Learn more about Arrowhead Research
Size
329 employees
Market Cap
$4 billion
Industry
Net Income
-$102.6 million
Founded
2004
5 Year Trend
+50.6%
Revenue
$79.8 million
NASDAQ

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