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Biotechnology Associate Director Jobs in California

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Associate Director, Biostatistics

San Diego, CA · On-site

$190.54 - $230.89/hr

... biotech with the global expertise and resources of a leading innovator in oncology. Our mission is ... Associate Director, Biostatistics Department: Biometrics Location: San Diego FLSA Status: Exempt ...

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Biotechnology Associate Director information

What does a biotechnology associate director do?

A Biotechnology Associate Director oversees research and development projects within biotech organizations, ensuring that scientific and business objectives are met. They manage teams of scientists and technical staff, coordinate cross-functional projects, and are responsible for regulatory compliance and quality assurance. Additionally, they play a key role in strategic planning, budgeting, and communicating progress to senior leadership. Their work helps guide the company’s innovation pipeline and ensures that products move efficiently from concept to market.

What are the key skills and qualifications needed to thrive as a biotechnology associate director?

To thrive as a Biotechnology Associate Director, you need advanced knowledge in molecular biology or related life sciences, extensive research experience, and a graduate degree (often a Ph.D.) in biotechnology or a similar field. Familiarity with laboratory information management systems (LIMS), regulatory compliance standards (like FDA or EMA), and project management tools is typically required. Strong leadership, strategic thinking, and communication skills distinguish top performers in this role. These competencies are crucial for leading teams, ensuring regulatory compliance, and driving the successful development of innovative biotech solutions.

What are some common challenges biotechnology associate directors face when leading cross-functional teams?

Biotechnology Associate Directors often navigate the complexities of coordinating efforts between research scientists, regulatory affairs, manufacturing, and commercial teams. One common challenge is aligning diverse priorities and timelines while ensuring compliance with strict industry regulations. Effective communication and adaptability are essential to foster collaboration, resolve conflicts, and keep projects on track. Successfully managing these dynamics leads to efficient product development and positive team outcomes.

What is the difference between Biotechnology Associate Director vs Biotechnology Scientist?

AspectBiotechnology Associate DirectorBiotechnology Scientist
Required CredentialsMaster's or PhD in Biotechnology, Life Sciences, or related field; extensive industry experienceMaster's or PhD; focus on research and development
Work EnvironmentLeadership roles in R&D teams, project management, strategic planningLaboratory research, experimental design, data analysis
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech divisionsResearch institutions, biotech companies, academia
Common Search & ComparisonOften compared for leadership and strategic rolesFocused on scientific research and experimentation

The Biotechnology Associate Director typically holds a leadership position overseeing research teams and strategic projects, requiring extensive experience and advanced degrees. In contrast, a Biotechnology Scientist primarily conducts laboratory research and experiments. Both roles are vital in biotech companies, but they differ in responsibilities, focus, and career level.

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

For Biotechnology Associate Director jobs in California, the most frequently searched job titles are:

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

The top searched job categories for Biotechnology Associate Director jobs in California are:

What cities in California are hiring for Biotechnology Associate Director jobs?

Cities in California with the most Biotechnology Associate Director job openings:

Biotechnology Associate Director jobs near you
Infographic showing various Biotechnology Associate Director job openings in California as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 23% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Associate Director, Clinical Pharmacology

Latigo Biotherapeutics

San Francisco, CA • On-site

$205K - $235K/yr

Full-time

Re-posted 16 days ago

Job description

Title: Associate Director, Clinical Pharmacology
Location: Thousand Oaks, CA or San Francisco, CA
Company Description:
Latigo Biotherapeutics, Inc. is a private, 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. We have a robust pipeline with programs ranging from preclinical to late phase. The company, whose headquarters is in Thousand Oaks, CA, with a satellite office in San Francisco, CA, has a highly successful management team as well as an experienced Board of Directors. At Latigo, we value honest science, patient-focus, and innovation.
Position Description:
Reporting to the Head of Clinical Pharmacology, the Associate Director, Clinical Pharmacology will work in our clinical development teams, with significant responsibility for the Clinical Pharmacology package of multiple clinical and Pre-IND programs. In this role, you will help formulate clinical pharmacology strategies from the FIH through registration.
Primary Responsibilities:
  • As part of the development team, you will provide expertise in the clinical development of small molecule programs, in particular the design and oversight for clinical pharmacology studies.
  • Lead and manage design and conduct of clinical pharmacology studies of increasing complexity.
  • Analyze, interpret and author documents for clinical submissions, including but not limited to clinical study protocols and reports, Investigator's Brochures, and the clinical pharmacology sections of regulatory submissions.
  • Interact with regulatory agencies (US and ex-US) as needed.
  • You will be accountable for study-to-program level clinical pharmacology aspects of compounds in the discovery to development stage.
  • You will be responsible for oversight and interaction with consultants and vendors assigned to support clinical pharmacology tasks including PK, PKPD, and clinical assay development.

Qualifications and Requirements:
  • PharmD or PhD in a relevant discipline preferred.
  • 8+ years of experience in Clinical Pharmacology supporting early development in a biotech or pharmaceutical organization.
  • Prior, robust clinical pharmacology experience with small molecules is required. Experience in the design and conduct of multiple types of Phase 1 studies (e.g. FIH, DDI, FE, rBA, etc.) preferred.
  • Proficiency with modern PK analysis software (e.g. Phoenix WinNonLin) required.
  • Knowledge of regulatory requirements for clinical pharmacology preferred.
  • Strong interpersonal skills, and ability to influence development program teams.
  • Excellent verbal and written communication skills, and ability to clearly convey complex concepts to technical and non-technical audiences preferred.
  • Ability to work independently in a dynamic and fast-paced environment.
  • Experience in therapeutic areas related to pain management preferred.
  • Experience with regulatory submissions in early and late development is preferred.

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