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 Clinical Data Entry Specialist

Details
Country: USA
Location: Malvern PA
Total applied: 40
Location:US-PA-Malvern

Base Pay:N/A
Employee Type:Full-Time Employee

Industry:Biotechnology Pharmaceutical Healthcare - Health Services

Manages Others:no
Clinical Data Entry Specialist

Responsibilities: To perform data entry, verification, logging, and filing of CRFs, CRF design, and perform testing and QC of databases. Develops test cases and tests database entry screens. Maintain standard data entry instructions,develop study-specific data entry instructions, performs database QC and design CRFs based on standards and specifications from clinical team.
REQUIREMENTS
Requirements: B.S. or B.A. and 1+ years of experience in pharmaceutical or clinical research or 3+ years of relevant experience in clinical research. Candidates with lesser education may qualify if experience is commensurate. Knowledge of basic medical terminology. Proof of accuracy and acceptable spelling in technical/clinical typing test. Extensive experience in at least two of the three functional areas (Data entry, Database QC, CRF Design). Experience with CRF design software, such as Framemaker or Word/PDF, is a plus.

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