Bioanalysis Strategy Lead, Associate Director

Latigo Biotherapeutics, Inc.

Thousand Oaks, Northern (CA, KY)

Hybrid

USD 180,000 - 240,000

Full time

14 days+
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Job summary

Latigo Biotherapeutics, Inc. is seeking an Associate Director, Bioanalysis to lead bioanalytical activities across discovery, nonclinical, and clinical development.

You will provide strategic and operational leadership for assay development, validation, and data interpretation, coordinating with CROs and internal teams. The ideal candidate has deep LC-MS/MS expertise, strong regulatory knowledge, and a track record of guiding cross-functional teams, with experience across small molecules and

Qualifications

  • Significant bioanalytical experience supporting drug discovery and development.
  • Experience managing outsourced bioanalytical activities and CRO/vendor oversight.
  • Familiarity with FDA, EMA, and ICH bioanalytical method validation guidance.
  • Ability to influence cross-functional teams and manage multiple programs.

Responsibilities

  • Develop and lead bioanalytical strategies across discovery to clinical development.
  • Serve as bioanalytical lead on cross-functional project teams and manage timelines.
  • Identify, select, and oversee CROs and external labs for analyses.
  • Ensure GLP/GCP compliance and support regulatory submissions.
  • Mentor scientists and drive bioanalytical capability growth.

Skills

Bioanalytical leadership
Outsourced bioanalysis
LC-MS/MS expertise
Regulatory guidance
Cross-functional collaboration

Education

Ph.D. in Analytical Chemistry or related field
M.S. in Analytical Chemistry or related field
B.S. in Chemistry or related field

Tools

LC-MS/MS

Job description

Latigo Biotherapeutics, Inc. is seeking an Associate Director, Bioanalysis to lead bioanalytical activities across discovery, nonclinical, and clinical development.

You will provide strategic and operational leadership for assay development, validation, and data interpretation, coordinating with CROs and internal teams. The ideal candidate has deep LC-MS/MS expertise, strong regulatory knowledge, and a track record of guiding cross-functional teams, with experience across small molecules and

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