Principal Scientist, In Vivo Pharmacology, Neurology

GondolaBio

• $173K — $205K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 6+ years in biopharmaceutical industry, focusing on in vivo pharmacology.
  • Preferred experience with small molecules and antisense oligonucleotides (ASOs).
  • Strong background in rare disease or developmental and epileptic encephalopathy (DEE) models.
  • Demonstrated intellectual curiosity through engagement with the scientific community.
  • Experience in designing pharmacology studies and coordinating external efforts.
  • Familiarity with IND-enabling studies and writing regulatory or technical reports.
  • Ability to work independently in a fast-paced biotech environment.

Responsibilities

  • Design and execute in vivo pharmacology studies for Neurology programs in rodents and non-human primates.
  • Collaborate with toxicology and translational teams to ensure data rigor and translatability.
  • Develop pharmacodynamic and efficacy assessments, troubleshoot assays, and QC data from CROs.
  • Manage CRO relationships and monitor study progress, identifying risks and presenting updates.
  • Analyze data from pharmacology endpoints, including PK/bioanalysis and efficacy assessments.

Benefits

  • Remote work flexibility or option to work in Palo Alto, CA.
  • Opportunity to work on cutting-edge Neurology programs.
  • Engagement with a collaborative and innovative team environment.
  • Involvement in IND submission processes and regulatory interactions.
Full Job Description
Job Type

Full-time

Description

Principal Scientist, In Vivo Pharmacology, Neurology

Remote U.S. or Palo Alto, CA

Key Responsibilities
  • Design and execute on in vivo pharmacology studies across multiple Neurology programs in our research portfolio in rodents and non-human primates, with goals of IND submission.
  • Partner with toxicology and translational teams to ensure our in vivo pharmacology data package is rigorous, reproducible, and translatable - directly informing dose selection and go/no-go decisions.
  • Develop and implement pharmacodynamic and efficacy assessments, troubleshoot assays, and QC data from CROs and external partners.
  • Manage CRO relationships and monitor study progress for ongoing studies, identifying emerging risks, while presenting progress updates in team meetings.
  • Analyze data from in vivo pharmacology endpoints including PK/bioanalysis and pharmacodynamic and/or efficacy endpoints.


Requirements

Preferred Education & Experience
  • Bachelor's degree and 6+ years of biopharmaceutical industry experience within in vivo pharmacology.
  • Experience with small molecules and antisense oligonucleotides (ASOs) is preferred.
  • Experience in rare disease or developmental and epileptic encephalopathy (DEE) models is strongly preferred.
  • Strong intellectual curiosity as demonstrated by routine engagement with scientific community and familiarity with literature.
  • Direct experience and willingness to continue to design pharmacology studies with direct involvement and leading coordination of external efforts.
  • Exposure to IND-enabling studies and experience writing regulatory or technical reports.
  • Ability to operate independently and cross-functionally in a lean, fast-moving biotech environment.

The base pay range for this position is $173,000 to $205,000 per year. The actual compensation offered will be determined based on a number of job-related factors, including experience, skills, qualifications, and location. A bonus plan and equity will also be offered.

Employees of BridgeBio and all affiliated companies should work through their managers to inquire about and learn more about this role.

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