Clinical Research Coordinator / Recruiter

Clinical Research Coordinator / Recruiter Scientist Include but are not Limited to the Following:

• Review Requests for Recruitment (RFR) upon receipt from Principal Investigator/Management.
• Review new subject profile, photo release, and HIPAA forms, assign an ECRL ID# to panelists.
• Process panelist profiles, entering new profiles, updates from returning panelists, medication changes and restriction notices into the Clinical Trial Management System (CTMS)
• Maintain autodial reminder calendar, distributing reminder calls to be made on a daily basis, process recruitment and automated calls at the request of the Department Manager or Team Lead
• Attend coordination meeting between Recruiting and other departments.
• Take note of and inform the Principal Investigator/Management of any unforeseen circumstances that may affect the quality and integrity of the study when they occur.
• Follow all protocols and SOPs relevant to recruiting and report any deviations promptly to Management.
• Train new recruiting department personnel in all aspects of the position. 
• Perform panelist payouts upon study completion.
• General recruiting duties as needed

Basic Minimum Education Qualifications:

• High school Diploma or GED.

Basic Minimum Work Requirements:

• Customer service experience or customer-facing experience, preferred 
• Ability to perform light computer work
  • Knowledge of Microsoft Office, Excel, 
    and Word
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Position is part-time working  Monday-Friday 8:00am - 5:00pm, with overtime as needed.  Candidates currently living within a commutable distance of Austin, TX are encouraged to apply

Eurofins USA Consumer Product Testing is a Disabled and Veteran Equal Employment Opportunity employer.