Lead Scientist 1, LC-MS

Labcorp • Madison, WI

8d

About The Position

Here at Labcorp, we have an opportunity for an experienced Bioanalytical Lead Scientist I to support our LC/MS Bioanalytical Study Team in Madison, WI.
At Labcorp, Drug Development's work in developing new pharmaceutical solutions has an incredible impact on the lives of millions worldwide. Join us & be a part of this life-saving work!
Bioanalytical Lead Scientist I - LCMS

Requirements

• Bachelors (BA/BS) degree in a science or related field (i.e. chemistry, biology etc.)
• 3-4 years of experience in the job discipline listed above
• 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
• Experience and skill with Watson, Nautilus, and Analyst
• Knowledge of regulatory agency guidelines

Nice To Haves

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

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.

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.
• Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level