External Data Reviewer at Labcorp Drug Development

About the job

Job Overview

External Data Reviewer

Get ahead in your career and make a difference in people's lives!

Are you a self-starter who knows how to take initiative in your daily work? Would you enjoy making a real difference in the lives of others? Are you looking to progress your career within Data Management?

If you are looking for a high-energy position in a collaborative environment, learn more about the External Data Reviewer opportunity with Labcorp.

• Ensure electronic vendor data contains all protocol-specified parameters, is in correct format and data populates to the specified fields and patients correctly.
• Assist in the development of the Data Transfer Agreement and Data Transfer Specifications for vendor data transfers.
• Review data discrepancies generated by study-specific edit checks for External data and perform the subsequent query management process in resolving the data issues.
• Perform validation review of the electronically transmitted data for a sample of the total number of patients in the study for loading purposes.
• Assist with review of External Data edit checks, External Data status reports, and External Data listings.
• 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.
• Responsible as a contact person for the External source of electronic data transmissions with initial oversight for support of this communication from EDS 2 or 3 levels.
• Communicate to vendors and client problems involving data transfers, data point issues and validation issues.
• Perform other duties as required by the Department

Education/Qualifications

• Medical Laboratory Technology certificate preferred
• Associates or Bachelor’s degree or relevant experience

Experience

• Minimum 1-3 years of experience, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job, involving data management or laboratory/trials experience.
• Knowledge of CRF would be advantageous
• Ability to maintain the confidentiality of data and information during interactions with staff at all levels
• Demonstrated computer literacy
• Accurate keyboarding skills
• Basic understanding of medical terminology
• Understanding of ICH-GCP principles

2021-70611

Covance is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.