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Bioanalytical Research Associate Jobs (NOW HIRING)

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Bioanalytical Research Associate information

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How much do bioanalytical research associate jobs pay per hour?

As of Jul 18, 2026, the average hourly pay for bioanalytical research associate in the United States is $32.54, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $37.02 per hour, depending on experience, location, and employer.

What is a bioanalytical science salary?

A Bioanalytical Research Associate typically earns a salary ranging from $50,000 to $80,000 annually, depending on experience, education, and location. The role often requires proficiency with analytical techniques and laboratory tools, with salaries increasing with specialized skills and certifications.

What can I do with an associate's degree in biochemistry?

A Bioanalytical Research Associate with an associate's degree in biochemistry can work in laboratories performing sample analysis, data collection, and method development. They often assist in research projects, operate laboratory equipment, and follow safety protocols, supporting scientists and researchers in various biotech and pharmaceutical settings.

Do I need a PhD to be a research associate?

A Bioanalytical Research Associate typically does not need a PhD; a bachelor's or master's degree in a relevant field such as biology, chemistry, or pharmacology is usually sufficient. Relevant skills include laboratory techniques, data analysis, and familiarity with analytical instruments. Advanced roles or research positions may require a higher degree, but entry-level positions often do not.

What are some common challenges faced by Bioanalytical Research Associates in managing multiple projects simultaneously?

Bioanalytical Research Associates often juggle several projects at once, each with unique timelines and experimental requirements. A key challenge is prioritizing tasks while ensuring data integrity and compliance with regulatory standards. Effective time management, clear communication with cross-functional teams, and staying organized are essential for meeting deadlines and maintaining high-quality results. Collaborating closely with colleagues in analytical, QA, and project management roles can help navigate shifting priorities and unexpected hurdles.

How do you become a bioanalyst?

To become a bioanalytical research associate, typically a bachelor's degree in biology, chemistry, or a related field is required, with many roles preferring or requiring a master's degree or higher. Gaining experience in laboratory techniques, such as chromatography or mass spectrometry, and familiarity with regulatory standards like GLP can enhance job prospects. Certifications or training in bioanalytical methods may also be beneficial for career advancement.

What is the difference between Bioanalytical Research Associate vs Laboratory Technician?

AspectBioanalytical Research AssociateLaboratory Technician
Required CredentialsBachelor's degree in life sciences, relevant certificationsAssociate's or Bachelor's degree in science or related field
Work EnvironmentResearch labs, pharmaceutical companies, biotech firmsClinical labs, research facilities, manufacturing plants
Employer & Industry UsageUsed in biotech, pharma, and research industries for analytical testingCommon in clinical, industrial, and research labs for sample processing

The main difference between a Bioanalytical Research Associate and a Laboratory Technician lies in their roles and responsibilities. Bioanalytical Research Associates focus on conducting complex analytical tests, data analysis, and supporting research projects, often requiring specialized knowledge. Laboratory Technicians typically handle routine sample preparation and testing tasks. Both roles are essential in scientific environments, but the Research Associate position generally involves more advanced analytical work and data interpretation.

What does a Bioanalytical Research Associate do?

A Bioanalytical Research Associate is responsible for conducting laboratory experiments and analyses to measure and study biological molecules, such as proteins, DNA, and metabolites. They typically use advanced techniques like mass spectrometry, chromatography, and immunoassays to support drug development, clinical trials, or scientific research. Their work ensures the accuracy and reliability of data used in regulatory submissions and scientific publications. Additionally, they maintain detailed records, follow strict safety protocols, and collaborate with other scientists to interpret results.

What are the key skills and qualifications needed to thrive as a Bioanalytical Research Associate, and why are they important?

To thrive as a Bioanalytical Research Associate, you need a solid background in chemistry, biology, or a related field, usually supported by a relevant bachelor's or master's degree. Familiarity with analytical techniques such as HPLC, LC-MS/MS, and laboratory information management systems (LIMS) is typically required. Strong attention to detail, problem-solving skills, and effective teamwork set candidates apart in this role. These competencies ensure accurate data generation, reliable results, and smooth collaboration within research and development teams.
More about Bioanalytical Research Associate jobs
What cities are hiring for Bioanalytical Research Associate jobs? Cities with the most Bioanalytical Research Associate job openings:
What states have the most Bioanalytical Research Associate jobs? States with the most job openings for Bioanalytical Research Associate jobs include:
Infographic showing various Bioanalytical Research Associate job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $67,685 per year, or $32.5 per hour.
DMPK and Bioanalytical Associate Director

DMPK and Bioanalytical Associate Director

Vertex Pharmaceuticals

Seattle, WA • On-site

$166K - $249K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 14 days ago


Job description

Job Description
General Summary:
The Associate Director, DMPK and Bioanalysis drives DMPK-related activities across multiple biotherapeutic programs. This role is recognized internally as an emerging leader in one or more disciplines within DMPK, as well as bringing technical expertise in bioanalytical assay development, validation, and CRO management. The Associate Director demonstrates scientific rigor and accountability, working collaboratively across functions and teams to ensure delivery of reliable, high-quality DMPK and bioanalytical data in support of Research and Development programs.
Key Duties and Responsibilities:
  • Acts as the DMPK and Bioanalytical Lead on multidisciplinary project teams, representing the integrated DMPK-BA perspective and clearly communicating data, risk assessments, and recommendations to project stakeholders
  • Shapes and delivers PK and bioanalytical strategies across a portfolio of biotherapeutic programs, generating high-quality data that directly informs development, translational, and regulatory decision-making from preclinical through clinical stages
  • Contributes scientific and strategic input to the design, execution, interpretation, and reporting of in vivo PK and PK/PD studies
  • Plans, implements, and manages a broad range of bioanalytical testing activities for biotherapeutic candidates in support of preclinical, clinical and pharmacology studies
  • Contributes to bioanalytical method development and phase-appropriate qualification and validation of assays (including ligand binding and cell-based PK, immunogenicity and biomarker assays), and oversees transfer of methods to CROs
  • Contributes to CRO evaluation, selection, and ongoing management, including participation in vendor audits, troubleshooting assay performance, and management of external collaborations
  • Contributes to preparation of regulatory data packages, dossiers, and responses in support of interactions with health authorities, audits, and inspections
  • Reviews and influences changes to systems, procedures, methods, and regulatory submissions to support continuous improvement across bioanalytical and development functions

Knowledge and Skills:
  • Deep expertise in DMPK and bioanalytical science, with demonstrated ability to integrate in vitro and in vivo data to inform compound progression and risk assessment
  • Knowledge of basic pharmacokinetics and experience working with common pharmacokinetics software (e.g., Phoenix WinNonlin)
  • Specialized depth of knowledge in bioanalytical assay development for large-molecule therapeutics, including ligand binding and cell-based PK, immunogenicity and biomarker assays
  • Strong understanding of phase-appropriate assay qualification and validation and method transfer to external laboratories
  • Demonstrated ability to provide scientific and technical leadership on complex, high-value project assignments
  • Strong experience working with CROs in regulated environments, including oversight of data quality and compliance with GLP/GxP and relevant regulatory standards
  • Working knowledge of quality systems and regulatory requirements (e.g., GLP/GxP, 21 CFR Part 11/210/211)
  • Ability to mentor and advise others on technically challenging bioanalytical strategies and execution
  • Strong written and verbal communication skills, with the ability to author and review advanced technical documents and effectively communicate scientific concepts to diverse audiences
  • Demonstrated initiative, persistence, and scientific creativity to advance development programs
  • Values teamwork and collaboration within cross-functional and external partnerships
  • Prior participation in regulatory inspections, audits, or health authority interactions preferred

Education and Experience:
  • Bachelor's, Master's, or PhD in Analytical Chemistry, Biochemistry, Protein Sciences, Chemistry, or a related scientific discipline
  • Bachelor's degree (or equivalent degree) and 11+ years of productive, relevant employment experience, or
  • Master's degree (or equivalent degree) and 9+ years of productive, relevant employment experience, or
  • Ph.D. (or equivalent degree) and 6-8+ years of productive, relevant post-doctoral employment experience

Pay Range:
$166,500 - $249,700
Disclosure Statement:
The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
Flex Designation:
On-Site Designated
Flex Eligibility Status:
In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time.
#LI-Onsite
Company Information
Vertex is a global biotechnology company that invests in scientific innovation.
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com