♦ Follow applicable departmental Standard Operating Procedures, Work Instructions and departmental guidelines. ♦ Complete required trainings according to required timelines. ♦ Complete day-to-day tasks ensuring quality and productivity. ♦ Create and modify clinical investigator manuals, requisitions and other relevant materials according to SOW requirements to provide on-time, quality project related documentation. ♦ Ensure that language translations of assigned project related documents are completed in a timely manner. ♦ Work effectively with peers to ensure delivery of appropriate DP documentation. ♦ Ensure timely escalation as needed. ♦ Other duties as assigned by management.
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. We encourage all to apply.
For more information about how we collect and store your personal data, please see our Privacy Statement (https://www.labcorp.com/hipaa-privacy/web-privacy-policy) .
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