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Full-Time

Principal Scientist

Large Molecule Pharmacokinetics

Posted on 4/19/2024

Denali Therapeutics

Denali Therapeutics

201-500 employees

Develops therapeutics for neurodegenerative diseases

Hardware
Biotechnology

Compensation Overview

$158k - $206.8kAnnually

Senior, Expert

San Bruno, CA, USA

Category
Computational Biology
Biology Lab & Research
Biology & Biotech
Requirements
  • PhD in pharmacokinetics, pharmacology/toxicology, immunology, biochemistry, engineering, or related field with industry/post-doctoral experience of 7+ years, or BS/MS with 12+ years.
  • Established expertise in large molecule pharmacokinetics, with experience in the biological factors and molecular physicochemical attributes that may impact PK and disposition.
  • Proven track record investigating PK/PD relationships for large molecule therapeutics, including analysis using appropriate software applications (i.e WinNolin, Watson, etc.).
  • Understanding of bioanalytical methods (ligand binding assays, mass spectrometry, or other biodistribution methodologies) to assess protein therapeutics PK and disposition in biological matrices.
  • Excellent critical thinking and scientific skills, and a demonstrated ability to analyze, interpret, and clearly communicate complex results.
  • Ability to work effectively and collaboratively on cross-functional project teams.
  • Excellent oral and written communication and presentation skills.
Responsibilities
  • Serve on teams as the PK expert contributing to the optimization and selection of lead candidates.
  • Support efforts to identify key aspects of target biology impacting PK properties and duration of PD response.
  • Perform PK/PD analyses to establish quantitative understanding of exposure-response.
  • Work closely with our bioanalytical scientists, biologics discovery, toxicology, clinical. pharmacology, and regulatory teams to optimize leads, to select candidates for clinical evaluation, and contribute to regulatory filings.
  • Analyze, interpret, summarize, and present PK and disposition data to internal project teams, senior management, and to global health authorities.
  • Prepare study protocols and coordinate execution of nonclinical PK or PK/PD studies to answer translational questions in support of project deliverables and first-in-human dose predictions.
  • Contribute to the design and TK analysis for non-GLP and GLP toxicology studies.
  • Work closely with project teams, line management and CROs to assure high quality and timely delivery of written reports for regulatory submissions.
  • Write, review, and finalize nonclinical PK sections of regulatory (IND/CTA) filings and contribute to clinical protocol development.

Denali Therapeutics specializes in developing molecular therapeutics for neurodegenerative diseases, leveraging expertise in the biology of these diseases and the blood-brain barrier. The company rigorously evaluates genetic targets and engineers brain delivery for therapeutic development.

Company Stage

IPO

Total Funding

$1.1B

Headquarters

San Francisco, California

Founded

2015

Growth & Insights
Headcount

6 month growth

-10%

1 year growth

-11%

2 year growth

-3%
INACTIVE