- Independently organizes and conducts routine analyses of samples and/or develops/validates methodologies for various compounds and components in compliance with standard operating procedures (SOPs) and regulatory
- Capable of complex analyses independently using new methods/technology and able to provide oversight and guidance to less experienced chemists.
- Documents work, maintains study documentation and laboratory records according to appropriate regulatory documentation practices. Also can perform QC review of data.
- Independently operates laboratory equipment, including system set up and general maintenance as directed by SOP. Capable of problem identification and issue resolution relating to equipment repair and submits work orders or maintenance requests as appropriate.
- May provide input and participate in project meetings. This can include leading the planning, prioritization, and scheduling of team tasks for timely completion of assigned projects.
- Informs Study Director, Lead Scientist, and/or management of any problems or deviations that may affect integrity of the data. Initiates the need for corrective actions of problems, drives communication between team members, and actively participates in scientific discussions.
- Contributes to a cohesive team environment. Plans individual assigned workload on a daily basis in coordination with team members, can effectively manage multiple assignments.
- Identifies technical issues and proactively communicates them to the study team. Leads the design of troubleshooting experiments, performs or assists others in the execution of experiments, and provides an evaluation of the data in addition to issue resolution.
- Leads or co-leads process improvement initiatives.
- Maintains a clean and safe laboratory work environment. Demonstrates understanding of Health and Safety compliance by ensuring that policies/SOPs and training are up to date.
- Authors or provides peer review for Policy, SOPs, Guides, and new processes and ensures alignment with regulatory guidelines.
- Is considered a subject matter expert in applicable areas for sample analysis, laboratory, or site processes.
- May train, mentor, or assist less experienced staff.
- Participates in client visits and communicates method related or technical information as needed
- Able to lead and direct scientific work to support internal/external methods and projects, of simple to moderate complexity.
- May 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 requirement
- 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.
- Evaluates data and tables to ensure regulatory guidelines and expectations are met.
- Reviews and edits reports for scientific accuracy and completeness.
- Provides technical support/technical input as needed.
- Assists with efforts to troubleshoot and solve assay problems.
- Recognizes the functions of different teams within Labcorp and seeks guidance when appropriate.
- Contributes to scientific investigations.
- Approve QA project specific inspections/audits
- Approve data archival
- Serves as the scientific point of contact for the client., with minimal assistance.
- Works with the client to determine project requirements.
- Assists with scientific directives for the study team.
- Identifies scientific issues or scope changes within the study.
- Communicates, monitors, and may assist scientific expectations with scientific staff.
- Promotes quality within the study team.
- Provides a technical resource for less experienced team members.
- Actively promotes collaboration within and across groups.
- Provides appropriate recognition to team members.
- Promotes a positive impression of Labcorp internally and within the industry
- Ability to plan, prioritize, and manage workload.
- Demonstrated ability to manage moderate to high volume study work.
- Takes accountability and demonstrates responsibility regarding scientific study conduct.
- Good knowledge of client requirements.
- Manages time effectively.
- Performs other related duties as assigned.
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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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