About this opportunity
StartX lists this TMF & Regulatory Documentation Specialist opportunity in northern, Kentucky. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Karius is seeking a Clinical Trial Associate to support CRAs and study teams by collecting, QCing, and QAing regulatory documents and by helping to set up and maintain the TMF per ICH-GCP. The role focuses on ensuring completeness and timely filing while communicating with sites to obtain missing documents.
The CTA will work under guidance, building proficiency in TMF standards, with travel up to 10-20% and a remote-friendly environment in the Bay Area.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.