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Contract Clinical EDC Study Support Specialist
| Details |
Country: USA
Location: NJ East Hanover
Total applied: 29
Relevant Work Experience: 2+ to 5 Years
Career Level: Experienced (Non-Manager)
Education Level: Bachelor's Degree
Job Type: Temporary / Contract / Project
Job Status: Full Time
Job Shift: First Shift (Day)
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Contract Clinical EDC Study Support Specialist
Contract Clinical EDC Study Support Specialist in East Hanover, NJ for large pharma company.
-This is a full time contract for at least 6 months.
Requirements:
-BS degree in Life Sciences, Statistics, Mathematics, Computer Science, Medical Informatics or equivalent. -Minimum 3 years of pharmaceutical industry clinical development experience in clinical data management, clinical programming and/or preparation of regulatory submissions.
-Good communication, documentation, planning, organizational analysis and problem solving skills.
Responsibilities:
-Provides ongoing support of EDC (electronic data capture) based clinical trials through the transformation of data from one database format to another, including programming in TableTrans, validation support for TableTrans diagrams, and executing diagrams on a production schedule as required by the clinical teams. -Advanced knowledge in the following disciplines:
-Database Support: Oracle (SQL and PL/SQL) and Clinical or equivalent clinical database management system (Database support).
-Database Conversion Tools: TableTrans or equivalent SQL database conversion and export tools.
-Knowledge of EDC applications, on-line and off-line electronic data collection systems, and eCRF design.
Keywords: EDC, New Jersey, Data Manager, Programmer, CDA, CDC, CRF, Clin*.
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