Principal Scientist, DMPK
Neurocrine BiosciencesAbout the role
Who We Are:
At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs.
What We Do:
Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis* and uterine fibroids,* as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X and Facebook. (*in collaboration with AbbVie)
About the Role:
Neurocrine’s Drug Metabolism and Pharmacokinetics (DMPK) team is searching for an experienced pharmaceutical scientist to lead the application of absorption, distribution, metabolism, excretion (ADME) science to advance our portfolio. Working on cross-functional teams, our group applies in silico, in vitro, and in vivo approaches to mechanistically study the pharmacokinetics, absorption, and disposition of small molecules, biologics, peptides, gene therapies, and other complex modalities. You will serve as a technical leader within the DMPK department and participate in all stages of ADME assessment, from initial compound screening through IND and NDA regulatory submissions. This role will require engagement in experimental design and data interpretation to deliver the discovery and development portfolio of investigational targets and novel therapeutics. The candidate will represent DMPK on Research and Development teams and regularly interface with internal and external colleagues to ensure timely and accurate dissemination of ADME information._
Your Contributions (include, but are not limited to):
Acts as a DMPK representative on project teams providing scientific and strategic input
Design, execute, and manage the conduct, interpretation, and reporting of in vitro drug metabolism data, in vivo PK studies, and PK-PD studies
Prepare data summaries and presents results to peers, colleagues, project teams and leadership
Oversee outsourcing partners of DMPK studies, ensuring partners adhere to contractual standards, within budget
Provides expert level contribution in the preparation and review of regulatory submissions
Integrate in vitro ADME, in vivo PK, and PK/PD endpoints with discovery biology data to define structure activity- and structure-property-relationships to guide optimization strategies
Develop data visualization strategies to ensure consistent data interpretation across project teams to drive portfolio decisions
Aid in ADME knowledge management
Effectively partner
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