Job Description
Primary Duties and Responsibilities :
Assist in the conduct of clinical trials as specified by the study protocol under the supervision of designated Principal Investigator and departmental management
Record observations, measurements, and test results, as required
Provide a professional experience to test subjects, and answer all inquiries, as appropriate
Assist in the preparation of test materials, as needed
Perform data entry and data review to ensure study quality
Adhere to all Standard Operating Procedures to ensure consistency and quality work across CRL
Efficiently time manage multiple projects
Succinctly communicate day to day project details to both department manager and Principal Investigator
Perform department specific procedures as qualified by training and evaluation of proficiency
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