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Bioanalytics Jobs in Massachusetts (NOW HIRING)

Bioanalytical Scientist

Lexington, MA · On-site

$39.50 - $49.75/hr

As a key scientific lead, you will orchestrate the bioanalytical lifecycle - from internal method innovation to global CRO oversight - ensuring high-quality data generation in a GLP/GCP environment.

Bioanalytical Scientist

Lexington, MA · On-site

$150 - $180/day

As a key scientific lead, you will orchestrate the bioanalytical lifecycle - from internal method innovation to global CRO oversight - ensuring high-quality data generation in a GLP/GCP environment.

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Bioanalytics information

See Massachusetts salary details

$15

$34

$57

How much do bioanalytics jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for bioanalytics in Massachusetts is $34.38, according to ZipRecruiter salary data. Most workers in this role earn between $21.01 and $43.85 per hour, depending on experience, location, and employer.

What is a Bioanalytics job?

A Bioanalytics job involves the quantitative and qualitative analysis of biological samples to support drug development, clinical trials, and diagnostic testing. Professionals in this field use techniques such as mass spectrometry, chromatography, and molecular biology assays to assess biomarkers, drug metabolism, and disease indicators. They work in pharmaceutical companies, biotech firms, research institutions, and healthcare settings to ensure data accuracy, regulatory compliance, and scientific integrity. Bioanalytical scientists collaborate with cross-functional teams to interpret results and contribute to medical and therapeutic advancements.

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

To excel in Bioanalytics, you need a solid background in biology, chemistry, or biochemistry, with experience in laboratory techniques and analytical methodologies. Familiarity with tools like mass spectrometry, chromatography, PCR, and laboratory information management systems (LIMS), as well as certifications such as GLP or GMP compliance, is highly advantageous. Strong problem-solving, attention to detail, and communication skills enable effective teamwork and data interpretation. These abilities are crucial for ensuring precise, reliable analysis and facilitating the progress of projects in environments like pharmaceuticals, biotechnology, or clinical research.

What are the typical daily responsibilities of someone working in Bioanalytics?

Professionals in Bioanalytics typically spend their days preparing and analyzing biological samples, performing complex assays, and ensuring results meet quality and regulatory standards. They often utilize advanced laboratory instruments, maintain meticulous data records, and collaborate closely with researchers, project managers, and quality assurance teams. The role may also involve troubleshooting technical issues, validating methods, and contributing to scientific reports or presentations. This hands-on and analytical work environment suits those who enjoy a mix of routine processes and scientific problem-solving.

What are the most commonly searched types of Bioanalytics jobs in Massachusetts? The most popular types of Bioanalytics jobs in Massachusetts are:
What job categories do people searching Bioanalytics jobs in Massachusetts look for? The top searched job categories for Bioanalytics jobs in Massachusetts are:
What cities in Massachusetts are hiring for Bioanalytics jobs? Cities in Massachusetts with the most Bioanalytics job openings:
Infographic showing various Bioanalytics job openings in Massachusetts as of July 2026, with employment types broken down into 85% Full Time, 9% Part Time, and 6% Contract. Highlights an 91% Physical, and 9% Remote job distribution, with an average salary of $71,505 per year, or $34.4 per hour.

Associate Director, Bioanalytical Sciences

Kailera Therapeutics, Inc.

Waltham, MA

Other

Re-posted 25 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

 

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

 

Education:

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