Denali Therapeutics logo
Biotechnology, Pharmaceuticals, Neurodegenerative Disease Research

Senior Principal Scientist, Translational Medicine

South San Francisco, CAOnsiteFull TimePrincipal$171,000–$223,000 /yrPosted 4 days agoVisa sponsorship available

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Required skills

  • biochemistry
  • neurobiology
  • molecular biology
  • pharmacology
  • biomarker assays
  • clinical study setting
  • BLA
  • NDA
  • IND
  • health authority interactions

Nice to have

  • orphan disease drug development
  • natural history studies
  • patient registries
  • accelerated approval submission
  • FDA meetings
  • Type B meetings

Role summary

Denali Therapeutics is a biotechnology company focused on developing therapeutics for neurodegenerative diseases, lysosomal storage disorders, and other serious diseases. They utilize a proprietary platform to deliver biotherapeutics across the blood-brain barrier. The Senior Principal Scientist, Translational Medicine will partner with leaders to set biomarker strategy for large-molecule programs, shape biomarker-driven clinical development plans, and apply expertise in drug development and regulatory science. This role involves leading cross-functional teams, designing and implementing biomarker assays, authoring regulatory submission documents, interpreting complex data, and representing the organization at scientific conferences. The position requires a PhD with 12+ years of industry/academic experience in a relevant scientific discipline, expertise in biomarker assay development and interpretation in clinical settings, and experience contributing to regulatory submissions.

Denali Therapeutics Inc. is a biotechnology company pioneering a new class of biotherapeutics designed to cross the blood-brain barrier (BBB) using its proprietary TransportVehicle™ platform. With the first FDA-approved biologic specifically designed to cross the BBB, a clinically validated delivery platform and a growing portfolio of therapeutic candidates across all stages of development, we are advancing toward our goal of delivering effective medicines to transform the lives of people living with neurodegenerative diseases, lysosomal storage disorders and other serious diseases. 


We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.


Partners with leaders across Discovery and Development to set biomarker strategy for large-molecule programs in rare, genetically defined, and neurodegenerative diseases. Shapes biomarker-driven clinical development plans that support dose selection, proof-of-concept, and deep patient phenotyping. Applies expert knowledge of drug development and regulatory science to move therapeutics through the clinic toward approval. Influences program direction and strengthens the organization’s scientific reputation in biomarker science.

Key Accountabilities / Core Job Responsibilities

  • Lead complex, cross-functional, and external biomarker research programs within Translational Medicine
  • Lead cross-functional teams that deliver therapeutic project team objectives
  • Define biomarker strategies that generate clinical evidence of target engagement, pathway engagement, and disease-biomarker modulation, including surrogate or intermediate endpoints that support accelerated approval
  • Direct the design, qualification, and implementation of biomarker assays in clinically relevant biosamples
  • Author biomarker strategy and data packages for BLAs and other regulatory submissions, including briefing documents and health authority responses
  • Interpret complex data sets and communicate results to scientific, clinical, and leadership audiences
  • Mentor and guide the scientific work of other scientists across lab and project teams
  • Advance expertise in rare disease biomarkers, including lysosomal storage disorders, and integrate knowledge of adjacent disciplines such as CNS disorders
  • Contribute to patent filings, diligence reports, publications, and regulatory documents
  • Represent the organization at scientific conferences and in academic partnerships

Qualifications / Skills


Required

  • Typically requires a PhD in a relevant scientific discipline (e.g., biochemistry, neurobiology, molecular biology, pharmacology) with 12+ years of industry and/or academic experience
  • Expertise in developing, executing, and interpreting complex biomarker assays in a clinical study setting
  • Experience contributing to regulatory submissions (e.g., BLA, NDA, IND), including biomarker sections and health authority interactions
  • Record of high-quality publications and/or presentations in rare disease, translational research, or biomarkers
  • Strong written, oral, and presentation skills for scientific and cross-functional audiences

Preferred

  • Experience in rare or orphan disease drug development, including lysosomal storage disorders, natural history studies, or patient registries
  • Direct experience supporting an accelerated approval submission or FDA/health authority meetings (e.g., Type B/C meetings)
Salary Range: $171,000.00 to $223,000.00 . Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at https://www.denalitherapeutics.com/careers

This compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future.
 

Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

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