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Bioanalytical Project Manager Jobs in Everett, WA

Vrtx

DMPK and Bioanalytical Associate Director

Seattle, WA · On-site

$166K - $249K/yr

... management. The Associate Director demonstrates scientific rigor and accountability, working ... Acts as the DMPK and Bioanalytical Lead on multidisciplinary project teams, representing the ...

Actalent

Scientist

Everett, WA · On-site

Experience using Watson laboratory or bioanalytical data management software. * Demonstrated ability to handle multiple projects simultaneously, prioritize work effectively, and meet deadlines.

Actalent

LC-MS Principal Scientist

Everett, WA

Experience using Watson laboratory or bioanalytical data management software. * Demonstrated ability to handle multiple projects simultaneously, prioritize work effectively, and meet deadlines.

Altasciences

Senior QA Auditor

Everett, WA

... bioanalytical laboratory qualifications. * Under supervision of a mentor/coach, performs the following tasks: interpretation of FDA, regulations; project management; regulatory guidance review ...

All JobsBioanalytical Project JobsBioanalytical Project Manager JobsBioanalytical Project Manager Jobs in Everett, WA

Bioanalytical Project Manager information

See Everett, WA salary details

$49.2K

$106.7K

$170.7K

How much do bioanalytical project manager jobs pay per year?

As of Aug 12, 2026, the average yearly pay for bioanalytical project manager in Everett, WA is $106,667.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,800.00 and $124,800.00 per year, depending on experience, location, and employer.

What does a bioanalytical project manager do?

A Bioanalytical Project Manager oversees and coordinates bioanalytical studies, ensuring that projects are completed on time, within budget, and according to regulatory standards. They act as the main point of contact between clients, laboratory teams, and regulatory agencies, managing study timelines, resources, and data quality. Their responsibilities include planning project activities, monitoring progress, troubleshooting issues, and reporting results to stakeholders. They play a critical role in drug development by ensuring that bioanalytical testing meets scientific and compliance requirements.

What are the key skills and qualifications needed to thrive as a bioanalytical project manager?

To thrive as a Bioanalytical Project Manager, you need a strong background in bioanalysis, project management experience, and typically a degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), regulatory guidelines (such as GLP/GCP), and project management tools like MS Project is essential. Excellent communication, leadership, and organizational skills help manage cross-functional teams and client expectations. These skills ensure the successful planning, execution, and delivery of complex bioanalytical projects within regulatory and timeline constraints.

What are some common challenges faced by bioanalytical project managers, and how can they be addressed?

Bioanalytical Project Managers often face challenges coordinating timelines across multiple stakeholders, such as laboratory teams, clients, and regulatory bodies. Managing shifting project priorities and ensuring data integrity under tight deadlines can also be demanding. To address these challenges, effective communication, proactive risk management, and strong organizational skills are essential. Regular status meetings, clear documentation, and building strong relationships with both internal and external partners help keep projects on track and ensure compliance with regulatory standards.

What is the difference between Bioanalytical Project Manager vs Bioanalytical Scientist?

AspectBioanalytical Project ManagerBioanalytical Scientist
CredentialsBachelor's or Master's in Life Sciences, PMP often preferredDegree in Biology, Chemistry, or related field; PhD or Master's common
Work EnvironmentProject teams, client meetings, coordination rolesLaboratory research, data analysis, method development
Employer & Industry UsagePharmaceutical, biotech companies, CROsResearch labs, pharmaceutical companies, CROs

The Bioanalytical Project Manager oversees project timelines, budgets, and client communication, ensuring successful completion. In contrast, the Bioanalytical Scientist focuses on experimental design, data collection, and method development. Both roles are essential in the bioanalytical industry but differ in responsibilities and daily tasks.

What are popular job titles related to Bioanalytical Project Manager jobs in Everett, WA? For Bioanalytical Project Manager jobs in Everett, WA, the most frequently searched job titles are:
What job categories do people searching Bioanalytical Project Manager jobs in Everett, WA look for? The top searched job categories for Bioanalytical Project Manager jobs in Everett, WA are:
What cities near Everett, WA are hiring for Bioanalytical Project Manager jobs? Cities near Everett, WA with the most Bioanalytical Project Manager job openings:
Bioanalytical Project Manager jobs near you
Infographic showing various Bioanalytical Project Manager job openings in Everett, WA as of June 2026, with employment types broken down into 82% Full Time, 17% Part Time, and 1% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $106,667 per year, or $51.3 per hour.

DMPK and Bioanalytical Associate Director

Vrtx

Seattle, WA • On-site

$166K - $249K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 6 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, highquality 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 DMPKBA 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 highquality data that directly informs development, translational, and regulatory decisionmaking 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 phaseappropriate 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 largemolecule therapeutics, including ligand binding and cell-based PK, immunogenicity and biomarker assays
  • Strong understanding of phaseappropriate assay qualification and validation and method transfer to external laboratories
  • Demonstrated ability to provide scientific and technical leadership on complex, highvalue 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 crossfunctional 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

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