Clinical Research Coordinator / Recruiter

About the role

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 20-34 hours per week . 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.

Your Match

How well this role fits your profile.

Company Intel

What employees say

Worked at Eurofins? Share your experience