Manages scientific investigations. * Approves QA project specific inspections. * Approves data ... more Bioanalytical Method Development and Validation Preferred Qualifications : * Masters (MS ...
Manages scientific investigations. * Approves QA project specific inspections. * Approves data ... more Bioanalytical Method Development and Validation Preferred Qualifications : * Masters (MS ...
Principal Investigator/Bioanalytical Lead Scientist I- (LC-MS)
Madison, WI · On-site
$80K - $95K/yr
Manages scientific investigations. * Approves QA project specific inspections. * Approves data ... more Bioanalytical Method Development and Validation Preferred Qualifications : * Masters (MS ...
Principal Investigator/Bioanalytical Lead Scientist I- (LC-MS)
Madison, WI · On-site
$80K - $95K/yr
Manages scientific investigations. * Approves QA project specific inspections. * Approves data ... more Bioanalytical Method Development and Validation Preferred Qualifications : * Masters (MS ...
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 ...
Quick apply
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 ...
Quick apply
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 ...
Operations Scientist II
Madison, WI · On-site
Conduct bioanalytical sample preparations * Document work and maintain study documentation and laboratory records. * Communicate with project managers, lead scientists, and supervisor on projects ...
Operations Scientist II
Madison, WI · On-site
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 ...
Operations Scientist - II
Madison, WI · On-site
Conduct bioanalytical sample preparations * Document work and maintain study documentation and laboratory records. * Communicate with project managers, lead scientists, and supervisor on projects ...
Operations Scientist - II
Madison, WI · On-site
Conduct bioanalytical sample preparations * Document work and maintain study documentation and laboratory records. * Communicate with project managers, lead scientists, and supervisor on projects ...
Quality Control Analyst
Madison, WI · On-site
$24.25 - $32.50/hr
Managing Complexity. Improving Lives. We provide medicines to address unmet patient needs, stemming ... May assist with or lead QC projects for process improvements. * May draft reports, plans and ...
Quality Control Analyst
Madison, WI · On-site
$24.25 - $32.50/hr
Managing Complexity. Improving Lives. We provide medicines to address unmet patient needs, stemming ... May assist with or lead QC projects for process improvements. * May draft reports, plans and ...
Quality Control Analyst
$24.25 - $32.50/hr
Managing Complexity. Improving Lives. We provide medicines to address unmet patient needs, stemming ... May assist with or lead QC projects for process improvements. * May draft reports, plans and ...
Quality Control Analyst
$24.25 - $32.50/hr
Managing Complexity. Improving Lives. We provide medicines to address unmet patient needs, stemming ... May assist with or lead QC projects for process improvements. * May draft reports, plans and ...
... BioAnalytical and DMPK, Clinical Pharmacology ad BioMarkers. The GxP Laboratory Systems ... Project Management certification Wisconsin pay range $90,000--$115,000 USD Arrowhead provides ...
Quick apply
... BioAnalytical and DMPK, Clinical Pharmacology ad BioMarkers. The GxP Laboratory Systems ... Project Management certification Wisconsin pay range $90,000--$115,000 USD Arrowhead provides ...
... BioAnalytical and DMPK, Clinical Pharmacology ad BioMarkers. The GxP Laboratory Systems ... Project Management certification Wisconsin pay range $90,000-$115,000 USD Arrowhead provides ...
... BioAnalytical and DMPK, Clinical Pharmacology ad BioMarkers. The GxP Laboratory Systems ... Project Management certification Wisconsin pay range $90,000-$115,000 USD Arrowhead provides ...
Clinical Molecular Geneticist (Laboratory Director level)
Marshfield, WI · On-site
$124K - $167K/yr
Support process improvement projects to drive cost savings, efficiencies, and productivity ... Ability to manage confidential information. * Effectively communicate cross-functionally to all ...
Clinical Molecular Geneticist (Laboratory Director level)
Marshfield, WI · On-site
$124K - $167K/yr
Support process improvement projects to drive cost savings, efficiencies, and productivity ... Ability to manage confidential information. * Effectively communicate cross-functionally to all ...
Clinical Molecular Geneticist (Laboratory Director level)
Marshfield, WI · On-site
$124K - $167K/yr
Support process improvement projects to drive cost savings, efficiencies, and productivity ... Ability to manage confidential information. * Effectively communicate cross-functionally to all ...
Clinical Molecular Geneticist (Laboratory Director level)
Marshfield, WI · On-site
$124K - $167K/yr
Support process improvement projects to drive cost savings, efficiencies, and productivity ... Ability to manage confidential information. * Effectively communicate cross-functionally to all ...
Bioanalytical Project Manager information
What does a Bioanalytical Project Manager do?
What are the key skills and qualifications needed to thrive as a Bioanalytical Project Manager, and why are they important?
What are some common challenges faced by Bioanalytical Project Managers, and how can they be addressed?
What is the difference between Bioanalytical Project Manager vs Bioanalytical Scientist?
| Aspect | Bioanalytical Project Manager | Bioanalytical Scientist |
|---|---|---|
| Credentials | Bachelor's or Master's in Life Sciences, PMP often preferred | Degree in Biology, Chemistry, or related field; PhD or Master's common |
| Work Environment | Project teams, client meetings, coordination roles | Laboratory research, data analysis, method development |
| Employer & Industry Usage | Pharmaceutical, biotech companies, CROs | Research 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.
$80K - $95K/yr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 27 days ago
Labcorp rating
6.6
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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About Labcorp
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
Burlington, NC, US
Year founded
1978