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Bioanalytical Cro Jobs in Wisconsin (NOW HIRING)

Product Marketing Manager

Madison, WI · On-site +1

$155K/yr

Eurofins recently celebrated 30 years of excellence in bioanalytical testing. * The company has ... CRO (Contract Research Organization) services. Eurofins US Food is seeking a creative, detail ...

Bioanalytical Cro information

What challenges do bioanalytical CRO professionals face, and how can they be addressed?

Professionals working in bioanalytical CROs often encounter challenges such as managing tight project timelines, ensuring regulatory compliance, and adapting to rapidly changing client requirements. Balancing multiple studies simultaneously requires strong organizational skills and effective communication with both internal teams and clients. To address these challenges, it is important to maintain clear documentation, stay updated on industry best practices, and foster a collaborative team environment to ensure high-quality, reproducible results.

What is the difference between Bioanalytical Cro vs Bioanalytical Scientist?

AspectBioanalytical CroBioanalytical Scientist
CredentialsTypically requires a degree in life sciences, pharmacology, or related fields; certifications vary by companyRequires a degree in biology, chemistry, or related fields; advanced degrees preferred
Work EnvironmentContract research organizations, pharmaceutical companies, or biotech firms; project-based workResearch labs, pharmaceutical companies, or academic settings; more independent research
Employer & Industry UsageCommonly hired for clinical trial support and regulatory studiesEngaged in experimental design, data analysis, and method development

While both roles require a background in life sciences, a Bioanalytical Cro primarily manages outsourced projects and client communication, whereas a Bioanalytical Scientist focuses on experimental work and data analysis within a lab setting.

What is a bioanalytical CRO?

Bioanalytical CROs, or Contract Research Organizations, are specialized companies that provide analytical testing services to support pharmaceutical, biotechnology, and medical device development. They focus on analyzing biological samples, such as blood, plasma, or tissue, to quantify drugs, metabolites, or biomarkers. These services are crucial for preclinical and clinical studies, ensuring accurate and reliable data for regulatory submissions. Bioanalytical CROs help companies save time and resources by offering expertise, advanced instrumentation, and compliance with industry regulations.

What skills and qualifications are needed to work in a bioanalytical CRO?

To thrive as a Bioanalytical CRO professional, you need a background in life sciences or chemistry, strong analytical laboratory skills, and often a relevant degree such as a BSc or MSc. Familiarity with technical tools like LC-MS/MS, chromatography software, and compliance with GLP/GCP standards is typically required. Attention to detail, problem-solving abilities, and effective teamwork are crucial soft skills in this field. These skills ensure accurate data generation, regulatory compliance, and successful execution of client-sponsored research projects.
What cities in Wisconsin are hiring for Bioanalytical Cro jobs? Cities in Wisconsin with the most Bioanalytical Cro job openings:
Infographic showing various Bioanalytical Cro job openings in Wisconsin as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Senior Manager, LC-MS Bioanalysis

Labcorp

Madison, WI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago


Labcorp rating

6.6

Company rating: 6.6 out of 10

Based on 1,136 frontline employees who took The Breakroom Quiz

97th of 120 rated laboratories


Job description

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world's most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you'll have the opportunity to do meaningful work, grow your career and make a real impact on people's health around the world. Together, we're improving health and improving lives.
Senior Manager, LC-MS Bioanalysis
Location: Madison, WI, On-Site
Work Schedule: Monday thru Friday
Lead the Future of Bioanalytical Science
Are you a proven leader in LC-MS bioanalysis with a passion for developing high-performing teams, advancing scientific excellence, and driving operational success? We are seeking a Senior Manager, LC-MS Bioanalysis to lead our Method Development and Validation functions, providing strategic and operational leadership within a fast-paced, regulated bioanalytical environment.
In this role, you will oversee teams responsible for developing, validating, and troubleshooting LC-MS/MS bioanalytical methods that support pharmaceutical clients worldwide. You will combine people leadership, scientific expertise, and client management to deliver high-quality results, drive innovation, and support the continued growth of the organization.
Job Responsibilities:
Leadership & People Management
  • Lead and develop teams of bioanalytical scientists focused on LC-MS method development and validation.
  • Provide performance management, coaching, career development, and succession planning for direct reports.
  • Establish training plans and ensure team readiness for current and future business needs.
  • Lead recruitment, onboarding, and retention initiatives for scientific staff.
  • Foster a collaborative, accountable, and inclusive team culture.

Scientific & Technical Leadership
  • Serve as a subject matter expert in LC-MS/MS bioanalysis.
  • Provide technical guidance for method development, method transfer, troubleshooting, validation, and sample analysis activities.
  • Support internal teams and clients through scientific consultation and problem-solving.
  • Stay current with emerging bioanalytical technologies, regulatory expectations, and industry best practices.
  • Partner with commercial and project teams on study strategy, feasibility assessments, and client interactions.

Operational Excellence
  • Ensure laboratory activities are appropriately resourced, scheduled, and executed to meet client timelines.
  • Monitor departmental metrics and drive continuous improvement initiatives.
  • Support forecasting, project costing, and revenue recognition activities.
  • Ensure compliance with GLP, GCP, SOPs, quality standards, and safety requirements.
  • Lead corrective and preventive actions as needed to address operational or client concerns.

Client Engagement
  • Build and maintain strong relationships with pharmaceutical clients.
  • Participate in sponsor meetings, scientific discussions, and business development activities.
  • Represent the organization at scientific conferences and industry events.

Qualifications
Minimum Requirements
  • Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
  • Significant experience, 5 years or more in regulated LC-MS bioanalysis, including method development and validation.
  • 5 years or more of demonstrated success leading scientific teams in a regulated laboratory environment.
  • 3 years or more experience working in a GLP, GCP, and bioanalytical regulatory requirements role.

Preferred Qualifications
  • Advanced degree (MS or PhD) in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
  • 6 years or more of experience managing people leaders in larger scientific organizations.
  • 5 years or more previous client-facing experience within a CRO or pharmaceutical setting.
  • 6 years or more experience driving operational improvements, business metrics, and laboratory productivity initiatives.
  • Documented scientific publications, conference presentations, or recognized technical expertise in bioanalysis.

Additional Job Skills
  • Excellent communication, interpersonal, and organizational skills.
  • GLP/GCP and bioanalytical regulatory requirements experience.

Why Join Us?
  • Lead a highly skilled team of bioanalytical scientists.
  • Influence strategy, innovation, and business growth.
  • Work with cutting-edge LC-MS technologies supporting drug development programs.
  • Engage with global clients and industry leaders.
  • Enjoy comprehensive benefits, professional development opportunities, and a collaborative culture focused on scientific excellence.

Salary: $130,000 - 160,000 annually
All job offers will be based on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.
The position is also eligible for an annual bonus under the Labcorp Bonus Plan.
(Bonuses are payable based on corporate and/or business segment performance and are subject to individual performance modifiers.)
Application Window: Position will be posted 7/27/26 thru 8/16/26.
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. Relocation assistance available. For more detailed information, please click 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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