ZipRecruiter

Log In

1

Director Bioanalytical Jobs (NOW HIRING)

Orum Therapeutics

$33.75 - $42.50/hr

Bioanalytical Scientist Chemistry Start Date: 6/15/2026 Location: Daejeon office, KR (Hybrid: Yes ... Execute an integrated role that bridges high-level scientific leadership and direct lab-based ...

Orum Therapeutics

Bioanalytical Scientist

Lexington, MA · On-site

$150 - $180/day

As a key scientific lead, you will orchestrate the bioanalytical lifecycle - from internal method ... Execute an integrated role that bridges high-level scientific leadership and direct lab-based ...

Orum Therapeutics

Bioanalytical Scientist

Lexington, MA

$39.50 - $49.75/hr

As a key scientific lead, you will orchestrate the bioanalytical lifecycle - from internal method ... Execute an integrated role that bridges high-level scientific leadership and direct lab-based ...

MSD

Bioanalytical Scientist

Gaithersburg, MD · On-site

The Bioanalytical Scientist functions as a Bioanalytical Principal Investigator (BPI), providing ... If applicable, establish and monitor direct report performance and development goals, assign ...

next page

Showing results 1-20

All JobsDirector Bioanalytical Jobs

Director Bioanalytical information

See salary details

$29.5K

$138.6K

$222K

How much do director bioanalytical jobs pay per year?

As of Jun 27, 2026, the average yearly pay for director bioanalytical in the United States is $138,649.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,000.00 and $179,000.00 per year, depending on experience, location, and employer.

What are the typical daily responsibilities of a Director Bioanalytical?

As a Director Bioanalytical, your daily responsibilities often include overseeing the planning and execution of bioanalytical studies, ensuring compliance with regulatory standards, and managing a team of scientists and support staff. You’ll review and interpret complex data, troubleshoot analytical challenges, and coordinate closely with project managers, regulatory affairs, and external partners. Additionally, you’ll be involved in developing and validating new analytical methods and contributing to strategic decisions that support drug development pipelines. This dynamic role combines hands-on scientific oversight with high-level team leadership and cross-functional collaboration.

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

To thrive as a Director Bioanalytical, you need advanced expertise in bioanalytical chemistry, method development, and regulatory compliance, typically supported by a graduate degree in a related scientific field. Familiarity with analytical platforms such as LC-MS/MS, laboratory information management systems (LIMS), and relevant regulatory guidelines (FDA, EMA) is essential. Strong leadership, project management, and effective communication skills distinguish top candidates in this role. These abilities are vital to overseeing complex studies, ensuring data integrity, and leading multidisciplinary teams in a high-stakes environment.

What is a Director Bioanalytical job?

A Director Bioanalytical oversees bioanalytical strategy, laboratory operations, and regulatory compliance for drug development and research. They manage assay development, validation, and sample analysis to support preclinical and clinical studies. This role requires expertise in bioanalytical techniques such as LC-MS/MS, ELISA, and biomarker analysis. Additionally, they ensure compliance with GLP/GCP guidelines and collaborate with cross-functional teams to drive scientific decision-making.

More about Director Bioanalytical jobs
What cities are hiring for Director Bioanalytical jobs? Cities with the most Director Bioanalytical job openings:
What states have the most Director Bioanalytical jobs? States with the most job openings for Director Bioanalytical jobs include:
What job categories do people searching Director Bioanalytical jobs look for? The top searched job categories for Director Bioanalytical jobs are:
Director Bioanalytical jobs near you
Infographic showing various Director Bioanalytical job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $138,649 per year, or $66.7 per hour.

DMPK and Bioanalytical Associate Director

Vrtx

Seattle, WA

$166K - $249K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 19 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

Apply