External Data Reviewer - Labcorp Drug Development

eg. Accountant or Accounting or Kempinski



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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.

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  • 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

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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.

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