Associate Lead Scientist - BioA (LC-MS)
About The Position
The Associate Lead Scientist here at Labcorp, supports the LC-MS Bioanalysis team in Madison, WI location. The Bioanalysis division are responsible for providing analytical testing services to key pharmaceutical and biotech clients to support toxicology and clinical studies. Associate Lead Scientist – BioA (LC-MS) Job Responsibilities: You will support the Study Director, Responsible Scientist, or Principal Investigator for non-regulated, GLP-regulated, and GCP-regulated bioanalysis studies Lead and direct scientific work to support internal methods and experiments Develop and review protocols and sample analysis plans Review data with the method development team to ensure methods are ready for validation Approve validation methods and reviews sample analysis methods Independently review and approve raw data Evaluate data and tables to ensure regulatory guidelines and expectations are met Review reports for scientific accuracy and completeness Provide technical support as needed Assist with efforts to troubleshoot and solve assay problems Assist with client communications regarding scientific direction Work with the client to determine project requirements Assist with scientific directives for the study team Identify scientific issues or scope changes within the study Communicate and monitor scientific expectations with scientific staff and clients Promote quality within the study team Provide a technical resource for less experienced team members
Requirements
- Bachelor of Science (BS) degree in science or related field
- 2-3 years of experience in the job discipline
- Able to utilize word processing, database, spreadsheet, and specialized software
- Experience and skill with Watson, Nautilus, and Analyst preferred
- Knowledge of regulatory agency guidelines
- Excellent communication and interpersonal skills
- Proven ability to prioritize and manage time
- Excellent attention to detail
Nice To Haves
- Masters (MS) degree in science related field
- 4-5 years of experience in the job discipline
Responsibilities
- Support the Study Director, Responsible Scientist, or Principal Investigator for non-regulated, GLP-regulated, and GCP-regulated bioanalysis studies
- Lead and direct scientific work to support internal methods and experiments
- Develop and review protocols and sample analysis plans
- Review data with the method development team to ensure methods are ready for validation
- Approve validation methods and reviews sample analysis methods
- Independently review and approve raw data
- Evaluate data and tables to ensure regulatory guidelines and expectations are met
- Review reports for scientific accuracy and completeness
- Provide technical support as needed
- Assist with efforts to troubleshoot and solve assay problems
- Assist with client communications regarding scientific direction
- Work with the client to determine project requirements
- Assist with scientific directives for the study team
- Identify scientific issues or scope changes within the study
- Communicate and monitor scientific expectations with scientific staff and clients
- Promote quality within the study team
- Provide a technical resource for less experienced team members
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.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
