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