External Data Specialist 3 Job in Pennsylvania (PA), Other Career, Full Time Jobs in Covance, Inc. a division of LabCorp®
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External Data Specialist 3 job in Philadelphia

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Covance, Inc. a division of LabCorp® jobs
Pennsylvania (PA), Philadelphia
Job Code:  2018-23893
Employer:  Covance, Inc. a division of LabCorp®
Category:  Other
Job Type:  Full Time

Location
Country:  United States
State:  Pennsylvania (PA)
City:  Philadelphia
Map: 
09/13/2018

Description
Job Overview
External Data Specialist
Full time
Remote from anywhere in the U.S. or Canada

JOB SUMMARY
Be responsible for review, maintenance and update of safety laboratory/external data received from central or local laboratories. Working to ensure departmental SOPs, guidelines and global standards are followed to maintain coding integrity and ensure consistency across all projects as appropriate

JOB RESPONSIBILITIES
- 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. 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.
- CRF design, User Acceptance Testing (UAT) data review, and query writing experience preferred

KEY SKILLS & BEHAVIORS
- Produces high quality work using SOPs, guidelines and technical standards as defined by the global technical group
- Keeps others informed of project and/or technical issues by pro-actively communicating across teams/functions
- Manages time effectively in order to produce a quality deliverable in expected timeframe
- Completes all tasks agreed upon with minimum supervision
- Anticipates changing priorities and demands and addresses them proactively

TRAINING AND EXPERIENCE
- Medical Laboratory Technology (preferred), Medical or Life Science Bachelor Degree or relevant experience
- 1-3 years previous laboratory or clinical experience preferred Education/Qualifications
TRAINING AND EXPERIENCE
- Medical Laboratory Technology (preferred), Medical or Life Science Bachelor Degree or relevant experience
- 1-3 years previous laboratory or clinical experience preferred Experience
TRAINING AND EXPERIENCE
- Medical Laboratory Technology (preferred), Medical or Life Science Bachelor Degree or relevant experience
- 1-3 years previous laboratory or clinical experience preferred
ref: (2018-23893)
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