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Bioanalytical Project Manager Jobs in Madison, WI

Understanding of ICH guidance relevant to bioanalytical studies and how it applies in a GLP/GCP environment. * Strong project management capabilities, including coordination of multiple studies and ...

Understanding of ICH guidance relevant to bioanalytical studies and how it applies in a GLP/GCP environment. * Strong project management capabilities, including coordination of multiple studies and ...

Conduct bioanalytical sample preparations * Document work and maintain study documentation and laboratory records. * Communicate with project managers, lead scientists, and supervisor on projects ...

Conduct bioanalytical sample preparations * Document work and maintain study documentation and laboratory records. * Communicate with project managers, lead scientists, and supervisor on projects ...

Conduct bioanalytical sample preparations * Document work and maintain study documentation and laboratory records. * Communicate with project managers, lead scientists, and supervisor on projects ...

Bioanalytical Project Manager information

See Madison, WI salary details

$44.8K

$97.3K

$155.7K

How much do bioanalytical project manager jobs pay per year?

As of Jul 17, 2026, the average yearly pay for bioanalytical project manager in Madison, WI is $97,296.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,600.00 and $113,900.00 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, and why are they important?

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 Madison, WI? For Bioanalytical Project Manager jobs in Madison, WI, the most frequently searched job titles are:
What job categories do people searching Bioanalytical Project Manager jobs in Madison, WI look for? The top searched job categories for Bioanalytical Project Manager jobs in Madison, WI are:
Infographic showing various Bioanalytical Project Manager job openings in Madison, WI as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $97,296 per year, or $46.8 per hour.
Principal Investigator/Bioanalytical Lead Scientist I- (LC-MS)

Principal Investigator/Bioanalytical Lead Scientist I- (LC-MS)

Labcorp

Madison, WI

$80K - $95K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 27 days ago


Labcorp rating

6.6

Company rating: 6.6 out of 10

Based on 1,122 frontline employees who took The Breakroom Quiz

81st of 105 rated laboratories


Job description

Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve health outcomes for people. With our global scale and deep expertise, you'll do meaningful work, grow your career and make a real impact. Together, we're improving health and improving lives.


Lead Scientist I & Principal Investigator to support our LC/MS Bioanalytical Study Teamin Madison, WI

Work Schedule - Mon-Fri (Day Shift)

Job Responsibilities:

  • Leads and directs scientific work to support external methods and projects.

  • Serves as an SD, RS, CS, LS, or PI for non-regulated, GLP-regulated, and GCP-regulated studies as applicable.

  • Ensures client programs meet Labcorp, client, and regulatory requirements in order to meet defined milestones along the drug development pathway.

  • Develops and reviews protocols and sample analysis plans.

  • Reviews data with the Method Development Team to ensure methods are ready for validation.

  • Approves validation methods and reviews sample analysis methods.

  • Independently reviews and approves raw data.

  • Ensures that any circumstances that may affect the quality and integrity of the study are identified and documented as the occur and appropriate corrective action is taken.

  • Effectively evaluates data and tables to ensure regulatory guidelines and expectations are met.

  • Reviews and approves reports for scientific accuracy and completeness.

  • Ensures on-time delivery of high quality data and reports.

  • Provides technical support as needed.

  • Leads efforts to troubleshoot and solve assay problems.

  • Recognizes the functions of different teams within Labcorp and seeks guidance when appropriate.

  • Manages scientific investigations.

  • Approves QA project specific inspections.

  • Approves data archival.

  • Evaluates new proposals for technical feasibility.

  • Supports scientific papers or posters which are published or presented at scientific meetings.

  • Serves as the scientific point of contact for the client.

  • Effectively works with the client to determine project requirements.

  • Leads preinitiation meetings when needed.

  • Gives scientific directives to the study team.

  • Identifies scientific issues or scope changes within the study.

  • Communicates and monitors scientific expectations with scientific staff and clients.

  • Proactively identifies ways to increase client satisfaction.

  • Participates in client visits as a scientific lead.

  • Responds to unscheduled deadlines, client needs, and crises without neglecting other responsibilities.

  • Assists clients with experimental design outside the scope of SOPs.

  • Develops and delivers compelling messages that connect with the audience.

  • Promotes quality within the study team.

  • Provides a technical resource for less experienced team members.

  • Actively promotes collaboration within and across groups.

  • Communicates successes and provides positive recognition to team members.

  • Promotes a positive impression of Labcorp internally and within the industry.

  • Provides technical and scientific guidance to clients and other departments.

  • Leads new employee training and develops training materials and schedules.

  • Identifies process improvement opportunities, participates in execution of initiatives.

  • Advocates Labcorp ethics, vision, and values; fosters a high-performance culture.

  • Participates in projects and tasks in addition to lead scientist responsibilities.

  • Regularly provides support to other lead scientists or project managers.

  • Mentors other employees.

  • Able to plan, prioritize, and manage workload for large and complex projects.

  • Demonstrated ability to manage high volume study work for key clients.

  • Takes accountability and demonstrates responsibility regarding scientific study conduct.

  • Good knowledge of client requirements.

  • Manages time effectively.

  • Performs other related duties as assigned.

Minimum Qualifications:

  • Bachelors Degree (Chemistry, Biology)

  • 3-4 years or more experience supporting lead scientific projects that support external methods and projects

  • 2 years or more Good Laboratory Practice (GLP) experience required

  • 2 years or more Liquid Chromatography Mass Spectrometry experience required

  • 2 years or more Bioanalytical Method Development and Validation

Preferred Qualifications :

  • Masters (MS) degree in science or related field preferred

  • 1 year or more experience Watson, Nautilus, and Analyst software

  • 1 year or more experience Root Cause Analysis

  • 2 years or more experience working with regulatory agency guidelines and SOP's

Additional Job Standards:

  • Excellent communication and interpersonal skills

  • Proven ability to prioritize and manage time

  • Excellent attention to detail

  • Able to utilize word processing, database, spreadsheet, and specialized software

#LI-SD1

Application Window: 6/26 thru 7/26/2026

Pay Range: $80k - $95k annually

All job offers will bebased on a candidate's skills and prior relevant experience, applicabledegrees/certifications,as well as internal equity and market data.

Benefits:

Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.For more detailed information, pleaseclick here.


Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.


We encourage all to apply

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