Maintain in-depth and up to date knowledge of national and international GLP/GCP regulations and their application to the work area. Demonstrate understanding of regulatory compliance by:
• Maintaining Training Record, ensuring appropriate CCLs are in place, and reading/training is always up to date
• Maintain and complete study documentation in compliance with regulatory guidelines (e.g. OECD, GxP, Home Office license) in departmental process
Applies expertise in complex data evaluation and interpretation for study reports.
Ability to review and approve critical aspects of a project/study, including procedures and analysis strategies. Monitors progress and status of assigned studies. Ensures that all experimental data, including observations of unanticipated responses to the test system, are accurately recorded and verified.
Has ownership of assigned projects with respect to meeting predefined timeline. To be responsible for on time delivery targets (protocols, results, reports, audit responses).
Demonstrate knowledge of assays and procedures to be able to discuss with support from trained personnel techniques/procedures within team and externally (e.g. during cross training, with clients/QA during inspections/audits) across multiple work streams
Perform peer review of reports
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.
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