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Bioanalytical Lab Director Jobs (NOW HIRING)

WuXi AppTec

Senior Scientist I, Bioanalytical

Cranbury, NJ · On-site

$93K - $127K/yr

Functions as a study director, principle investigator, or project coordinator including serving as ... Must be able to work in Lab setting with exposure to biohazards / chemicals * Must be able to wear ...

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Bioanalytical Lab Director information

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$45K

$126.1K

$186K

How much do bioanalytical lab director jobs pay per year?

As of Sep 10, 2026, the average yearly pay for bioanalytical lab director in the United States is $126,086.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,000.00 and $138,500.00 per year, depending on experience, location, and employer.

What does a bioanalytical lab director do?

A Bioanalytical Lab Director oversees the daily operations, quality control, and scientific direction of a laboratory that analyzes biological samples. They are responsible for ensuring that all testing meets regulatory standards, managing laboratory staff, and developing protocols for new assays. Additionally, they collaborate with clients, oversee budget and resource allocation, and ensure data integrity and compliance with industry guidelines. This role requires strong leadership, extensive experience in bioanalysis, and a thorough understanding of laboratory best practices.

What are the key skills and qualifications needed to thrive as a bioanalytical lab director?

To thrive as a Bioanalytical Lab Director, you need advanced expertise in analytical chemistry, bioanalysis, and laboratory management, typically supported by a relevant PhD or master's degree and significant industry experience. Familiarity with regulatory standards (GLP, GCP), laboratory information management systems (LIMS), and instrumentation such as LC-MS/MS is crucial. Leadership, problem-solving, and effective communication are vital soft skills for managing teams and collaborating with clients or regulatory bodies. These skills ensure accurate results, regulatory compliance, and efficient lab operations, which are critical for the success of bioanalytical projects.

What are some unique challenges faced by a bioanalytical lab director, and how can they be addressed?

A Bioanalytical Lab Director often encounters challenges such as managing complex regulatory compliance, ensuring data integrity, and coordinating cross-functional teams. Balancing the need for high-quality results with tight project timelines and evolving client requirements can be demanding. Addressing these challenges requires strong leadership, a thorough understanding of industry guidelines (such as GLP and FDA regulations), and effective communication skills. Proactively investing in staff training and fostering a collaborative environment also help maintain high performance and adaptability within the team.

What are popular job titles related to Bioanalytical Lab Director jobs?

For Bioanalytical Lab Director jobs, the most frequently searched job titles are:

Infographic showing various Bioanalytical Lab Director job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, 1% Temporary, and 1% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $126,086 per year, or $60.6 per hour.

Sr. Principal Scientist / Director, DMPK & Bioanalytical Sciences

Cambridge, MA • On-site

Alltrna
Biotechnology Research and Development • 11 - 50 employees
Learn more about Alltrnaexternal

$179K - $236K/yr

Full-time

Medical, Retirement

Re-posted 3 days ago

Job description

Reporting to the Chief Scientific Officer, this role leads DMPK and bioanalytical strategy across nonclinical and clinical programs, operating as a hands-on scientific leader. We are looking for an accomplished DMPK and bioanalytical scientist with experience in PK study design, bioanalytical method development, and translational biomarker strategy. This person will support pharmacology and nonclinical toxicology programs, providing broader context across the nonclinical development portfolio. The ideal candidate brings deep scientific expertise and a hands-on approach and thrives in the fast-paced environment of a clinical-stage biotech where both scientific and strategic contributions are expected

Responsibilities

  • Lead DMPK and bioanalytical strategy across nonclinical and clinical programs, including PK, biomarker, and translational PD readouts

  • Lead method development, qualification, and validation for bioanalytical assays (GLP/GCP-compliant as required)

  • Design, execute, and oversee PK and PK-PD studies of tRNAs to evaluate delivery technologies (LNP and others) and biomarker effects

  • Manage and qualify CRO and external lab partners across bioanalytical and PK programs

  • Support nonclinical toxicology programs in collaboration with internal teams and CROs

  • Analyze, interpret, and present DMPK and translational biomarker data to internal leadership and external stakeholders

  • Author nonclinical sections of regulatory filings (e.g., IND) and briefing documents; support agency interactions and responses

  • Serve on the Research Leadership Team; represent DMPK and bioanalytical sciences in cross-functional program discussions

  • Manage and develop direct report(s); collaborate with the broader pharmacology team

Required Qualifications

  • PhD or equivalent in pharmacokinetics, pharmacology, biochemistry, analytical chemistry, or related field

  • 8+ years of industry experience in DMPK, bioanalytical sciences, or closely related function

  • Experience with a range of bioanalytical methods and their development, qualification, and validation in both nonclinical and clinical contexts (e.g. mass spectroscopy, ELISA, NGS, etc.)

  • Experience with ligand binding assays and multiplex immunoassay platforms (e.g., MSD, Luminex) for cytokine, immunogenicity, and biomarker analysis

  • Demonstrated CRO oversight - vendor qualification, study monitoring, data review

  • Experience designing and overseeing PK and PK-PD studies for novel delivery modalities; LNP experience preferred

  • Experience in translational or clinical biomarker development, including assay strategy and fit-for-purpose qualification

  • Strong scientific writing skills - regulatory documents (e.g., IND nonclinical sections) and internal study reports

  • Experience supervising and developing scientists

Preferred Qualifications

  • Experience in rare disease, genetic medicine, or nucleic acid / RNA therapeutics

  • Familiarity with LNP platform biology and delivery landscape

  • Familiarity with GLP toxicology study design and ICH nonclinical guidelines

  • Experience operating in a cross-functional leadership role at a clinical-stage biotech

  • Experience with LC-MS/MS or related mass spectrometry platforms

About Alltrna 

Alltrna is the first clinical-stage biotech company advancing tRNA medicines to address shared disease-causing mutations across many indications. The company's initial therapeutic programs are designed to restore full-length protein production in diseases caused by premature termination codons (PTCs), collectively referred to as Stop Codon Disease, which affects approximately 10% of people with a rare genetic disease. Alltrna's lead program, AP003, is a chemically modified, engineered tRNA oligonucleotide encapsulated in a clinically validated, liver-directed lipid nanoparticle. AP003 is being developed for the arginine-to-TGA (Arg-TGA) PTC in patients with liver Stop Codon Disease, including phenylketonuria, organic acidemias, and urea cycle disorders. Founded in 2018 by Flagship Pioneering, Alltrna has built an integrated platform to design, optimize, and deliver engineered tRNA therapeutics. 

For more information, visit www.alltrna.com

The salary range for this role is $179,000 - $236,000. Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Alltrna currently offers healthcare coverage, annual incentive program, retirement benefits and a broad range of other benefits. Compensation and benefits information is based on Alltrna's good faith estimate as of the date of publication and may be modified in the future.

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