Overview
In this role, you ensure GLP and GCP compliance across studies, performing protocol, data, and report audits while upholding SOPs. You will engage with operational teams to support RCQA responsibilities and contribute to local quality initiatives. The position combines regulatory guidance with cross-functional collaboration, offering impact on study integrity and process efficiency. This onsite, office-based role anchors Labcorp’s commitment to quality and compliant research practices.
Pay / Benefits
- Competitive salaries
- No weekend work
- Pension
- Generous holiday allowance
Responsibilities
- Conduct protocol reviews, data and report audits, and process inspections to GLP and GCP requirements
- Follow applicable policies and SOPs
- Interpret and apply regulatory regulations appropriately
- Explain the QA role sufficiently for client audits
- Build strong relationships with operational colleagues
- Ensure RCQA responsibilities are followed per controlled documents
- Collaborate with operational management on Quality topics and QA projects
- Contribute to local quality initiatives and process improvements to enhance compliance and efficiency
Key requirements
- Auditing experience or familiarity with study processes in the scientific industry
- Knowledge of regulatory requirements to GLP, GxP, or GCP
- Excellent attention to detail and organizational/process-improvement skills
- Ability to work independently and with others
- Strong verbal and written communication skills
- Experience using Microsoft Office: Outlook, Word, SharePoint, PowerPoint, Excel
- attention to detail
- strong communication
- team collaboration
- problem-solving
- GLP/GCP/GxP knowledge
- Microsoft Office suite
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