Senior Manager, LC-MS Bioanalysis

Labcorp•Madison, WI

13d•$130,000 - $160,000•Onsite

About The Position

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.

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.
Excellent communication, interpersonal, and organizational skills.
GLP/GCP and bioanalytical regulatory requirements experience.

Nice To Haves

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.

Responsibilities

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.
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.
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.
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.