CLINICAL DATA COORDINATOR
Summary: Responsible for the creation of all Data Management study documents. The main role would be to design, edit and arrange printing of the Case Report Forms (CRFs) for each clinical trial supported by Data Management. Creates study specific database documentation, data entry instructions, data management manuals and training materials which are based on study protocols and using templates. Assists the Associate Director and Manager in creating general Data Management guidelines and training materials, and in compiling data import and export documentation. Minimum Qualifications: Associates Degree in a related field from an accredited college or university and one (1) to two (2) years directly related and progressively responsible experience. Knowledge of medical terminology very desirable. Physical Requirements and Working Conditions: Incumbents in this class are subject to extended periods of sitting, standing and walking, vision to monitor, moderate noise levels. Work is performed in an office environment.
SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
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