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Director Bioanalytical Science Jobs (NOW HIRING)

What You'll Do The Director of Bioanalytical Sciences at MBX Biosciences is expected to provide strategic, scientific, and operational leadership for the development, validation, and execution of ...

What You'll Do The Director of Bioanalytical Sciences at MBX Biosciences is expected to provide strategic, scientific, and operational leadership for the development, validation, and execution of ...

Director, Bioanalytical Laboratory

Gaithersburg, MD ยท On-site

$114K - $149K/yr

... directing the resources of a bioanalytical laboratory performing assay validations and sample ... D. in Biology, Chemistry, or related scientific discipline is preferred. o Master's degree may be ...

Director, Bioanalytics

San Francisco, CA ยท On-site

$203K - $284K/yr

THE OPPORTUNITY Vir Biotechnology is seeking an experienced Director, Bioanalytical Science to provide scientific, technical, and regulatory leadership and expertise to develop, validate and ...

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Director Bioanalytical Science information

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How much do director bioanalytical science jobs pay per year?

As of Sep 12, 2026, the average yearly pay for director bioanalytical science in the United States is $111,876.00, according to ZipRecruiter salary data. Most workers in this role earn between $98,000.00 and $125,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Director Bioanalytical Science job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $111,876 per year, or $53.8 per hour.

Associate Director, Bioanalytical Sciences

Waltham, MA โ€ข On-site

Full-time

Re-posted 24 days ago


Job description

What You'll Do:

The Associate Director, Bioanalytical Sciences at Kailera Therapeutics will report to the Director, Bioanalytical Sciences and will be responsible for designing and executing bioanalytical strategies to support development programs for patients with obesity-related diseases. This role will oversee GLP-compliant bioanalytical work for non-clinical and clinical studies. The Associate Director will manage CRO-outsourced bioanalysis to advance drug candidates through various development stages while partnering with cross-functional teams to ensure the seamless integration of data into Kailera's broader development programs.

Required location: Waltham, MA (hub-based, onsite 3-4 days per week)

Responsibilities:

  • Lead bioanalytical strategy and execution in clinical and non-clinical studies
  • Collaborate with cross-functional teams to design and implement bioanalytical aspects of clinical development programs
  • Identify, select, and oversee CROs, ensuring adherence to timelines, budgets, and regulatory requirements
  • Manage and oversee outsourced bioanalysis of small molecules, peptides, and biomarkers
  • Direct the development, validation, and implementation of bioanalytical assays
  • Review validation protocols, test procedures, raw data, and technical reports to ensure scientific rigor and compliance with regulatory guidelines
  • Provide leadership in ensuring GLP compliance for bioanalysis in both non-clinical and clinical trials
  • Author and review bioanalytical sections of regulatory submissions
  • Represent the bioanalytical function in cross-functional project teams

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Required Qualifications:

  • 10+ years of relevant industry experience in bioanalytical sciences with a Bachelor's degree or 5+ years with an advanced degree
  • Expertise in regulated bioanalysis and clinical-stage drug development
  • In-depth knowledge of GLP/GCP requirements and industry best practices in bioanalytical laboratories
  • Proven experience in the regulatory requirements for method development and validation
  • Strong track record of managing CRO-outsourced bioanalysis and vendor relationships
  • Excellent project management skills with the ability to manage multiple priorities effectively
  • Experience with regulatory interactions is highly desirable
  • Experience contributing to regulatory filings for biologics and small molecules

Preferred Qualifications:

  • Experience with GLP-1 receptor agonists or related therapeutic areas
  • Strong understanding of bioanalytical considerations for incretin-based therapies

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Education:

  • Bachelor's degree in a relevant scientific discipline required (e.g., bioanalytical chemistry, pharmacology, or related field); PhD preferred