Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.
Did you know?
In July 2022, Labcorp announced its intention to spin off its clinical development business as a separate public company, subject to the satisfaction of certain customary conditions. Fortrea will become the new brand identity for our Clinical Development business in connection with the spin-off, which is expected in mid-2023.
We believe that the exceptional is possible when you have the right partner, so we are looking for the right people to help build a transformative force in Clinical Development. www.fortrea.com
Job Description:
Ensure electronic lab data contains all protocol specified lab parameters, is in correct format and data populates to the specified fields and patients correctly.
Review data discrepancies generated by study specific edit checks for laboratory data and assist in preparation of data clarification forms sent to the site or the central lab. Also, review missing/updated central laboratory data for potential request and substitution of local laboratory data.
Perform 100% validation review of the electronically transmitted data for 5% of total number of patients in the study for loading purposes.
Assist CDM Manager with review of laboratory edit checks, laboratory status reports and laboratory listings as necessary. Interact with Clinical staff (CTM/CRA) to obtain local laboratory normal ranges for all sites.
Research and resolve discrepant information concerning the normal ranges, and maintain proper documentation. Enter and perform QC for local laboratory normal ranges.
Verify the normal ranges are properly attached to the patient results in the local lab data collection module of the database.
Perform other duties as required by the Department Responsible as contact person for the External source of electronic data transmissions.
Keep the Central lab and client informed of problems involving data transfers, data point issues and validation issues.
Education/Qualifications:
B.Sc/M.Sc Life Science or equivalent
Experience:
3-5 years of relevant experience.
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.
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