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Director Bioanalytical Jobs in California (NOW HIRING)

TCWGlobal

Bioanalytical Scientist

San Diego, CA · On-site +1

$54.48/hr

Bioanalytical Scientist Pay Rate: Up to $54.48/hour Duration: 12-Month Assignment Hours: Full-Time Location: Remote Summary We are seeking a Bioanalytical Scientist to support scientific research and ...

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All JobsBioanalytical JobsDirector Bioanalytical JobsDirector Bioanalytical Jobs in California

Director Bioanalytical information

See California salary details

$28.9K

$135.8K

$217.4K

How much do director bioanalytical jobs pay per year?

As of Sep 4, 2026, the average yearly pay for director bioanalytical in California is $135,770.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,151.00 and $175,282.00 per year, depending on experience, location, and employer.

What is a director bioanalytical?

A Director Bioanalytical oversees bioanalytical strategy, laboratory operations, and regulatory compliance for drug development and research. They manage assay development, validation, and sample analysis to support preclinical and clinical studies. This role requires expertise in bioanalytical techniques such as LC-MS/MS, ELISA, and biomarker analysis. Additionally, they ensure compliance with GLP/GCP guidelines and collaborate with cross-functional teams to drive scientific decision-making.

What are the typical daily responsibilities of a director bioanalytical?

As a Director Bioanalytical, your daily responsibilities often include overseeing the planning and execution of bioanalytical studies, ensuring compliance with regulatory standards, and managing a team of scientists and support staff. You’ll review and interpret complex data, troubleshoot analytical challenges, and coordinate closely with project managers, regulatory affairs, and external partners. Additionally, you’ll be involved in developing and validating new analytical methods and contributing to strategic decisions that support drug development pipelines. This dynamic role combines hands-on scientific oversight with high-level team leadership and cross-functional collaboration.

What are the key skills and qualifications needed to thrive in the director bioanalytical position, and why are they important?

To thrive as a Director Bioanalytical, you need advanced expertise in bioanalytical chemistry, method development, and regulatory compliance, typically supported by a graduate degree in a related scientific field. Familiarity with analytical platforms such as LC-MS/MS, laboratory information management systems (LIMS), and relevant regulatory guidelines (FDA, EMA) is essential. Strong leadership, project management, and effective communication skills distinguish top candidates in this role. These abilities are vital to overseeing complex studies, ensuring data integrity, and leading multidisciplinary teams in a high-stakes environment.

What are popular job titles related to Director Bioanalytical jobs in California?

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What job categories do people searching Director Bioanalytical jobs in California look for?

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What cities in California are hiring for Director Bioanalytical jobs?

Cities in California with the most Director Bioanalytical job openings:

Director Bioanalytical jobs near you
Infographic showing various Director Bioanalytical job openings in California as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, 1% Temporary, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $135,770 per year, or $65.3 per hour.

Associate Director, Bioanalytics

Latigo Bio

San Francisco, CA • On-site

Full-time

Posted 2 days ago

New

Job description

Job Title: Associate Director, Bioanalytics

Location: Thousand Oaks, CA or San Francisco, CA

Reporting to: VP, Translational Science


Company Description: 

Latigo Biotherapeutics, Inc. is an early-stage biotechnology company focused on discovering and developing the next generation of non-opioid medicines for pain and pain-related syndromes. Our mission is the development of novel therapies that transform the lives of patients. The company is headquartered in Thousand Oaks, CA and has a highly successful management team and an experienced Board of Directors. At Latigo, we value science, patient-focus, and innovation. 


Position Description: 

Latigo is seeking an experienced and highly motivated Associate Director, Bioanalytics to lead bioanalytical activities supporting discovery, nonclinical, and clinical development programs. This individual will provide strategic and operational leadership for bioanalytical assay development, validation, and sample analysis activities conducted through external CRO partners and internal collaborators.

The successful candidate will serve as the bioanalytical subject matter expert across multiple programs and will work closely with Clinical Pharmacology, Biomarkers, Toxicology, DMPK, Clinical Operations, Regulatory Affairs, and Quality teams to ensure delivery of high-quality bioanalytical data that support key development decisions and regulatory submissions.

The ideal candidate will possess deep expertise in ligand binding assays, LC-MS/MS methodologies, biomarker assay platforms, and regulatory expectations for bioanalytical method validation. Experience supporting both small molecule and biologic drug development programs is desirable.


Key Responsibilities:


Bioanalytical Strategy & Leadership

  • Develop and execute bioanalytical strategies to support discovery, nonclinical, and clinical development programs.
  • Serve as the bioanalytical lead on cross-functional project teams.
  • Contribute to overall development strategy, timeline planning, and risk assessment activities.


CRO and Vendor Management

  • Identify, select, and manage CROs and laboratory service providers.
  • Oversee bioanalytical method development, qualification, validation, transfer, and sample analysis activities.
  • Review study plans, protocols, validation reports, and analytical data packages.
  • Ensure timely delivery of high-quality data and compliance with project timelines and budgets.


Regulatory & Quality Compliance

  • Ensure bioanalytical activities are conducted in accordance with GLP, GCP, and applicable regulatory guidance.
  • Author and review bioanalytical sections of regulatory submissions, including INDs, CTAs, briefing packages, IBs, and NDAs.
  • Support regulatory agency interactions and responses related to bioanalytical methodologies and data.
  • Collaborate with Quality Assurance to oversee inspections, audits, deviations, investigations, and CAPAs.


Data Review & Interpretation

  • Collaborate with Clinical Pharmacology, DMPK, and Biomarker teams to integrate bioanalytical findings into study and program assessments.
  • Present results and recommendations to project teams, senior leadership, and external stakeholders.


Team Collaboration & Development

  • Establish strong partnerships across Research, Development, Clinical, Regulatory, and CMC functions.
  • Mentor junior scientists and contribute to the growth of bioanalytical capabilities within the organization.
  • Foster a culture of scientific excellence, accountability, collaboration, and continuous improvement.


Qualifications


Education

  • D. in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, Molecular Biology, Pharmacology, or a related scientific discipline with 8+ years of relevant industry experience; or
  • S. degree with 12+ years of relevant industry experience; or
  • S. degree with 15+ years of relevant industry experience.


Experience

  • Significant bioanalytical experience supporting drug discovery and development for small molecule programs in the biotechnology or pharmaceutical industry.
  • Demonstrated expertise managing outsourced bioanalytical activities.
  • Extensive experience with LC-MS/MS methodologies for small molecule quantitation.
  • Strong understanding of FDA, EMA, and ICH bioanalytical method validation guidance.
  • Experience supporting regulatory filings and interactions.
  • Proven ability to influence cross-functional teams and manage multiple programs simultaneously.


Preferred Qualifications

  • Experience supporting Phase 1 through Phase 3 clinical studies.
  • Experience with pain, neuroscience, ion channel, or CNS drug development programs.

Core Competencies

  • Strategic thinking and scientific leadership
  • Strong project management and organizational skills
  • Excellent written and verbal communication abilities
  • Collaborative and team-oriented mindset
  • Sound judgment and decision-making
  • Ability to thrive in a fast-paced, entrepreneurial biotech environment