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.
#J-18808-LjbffrTMF & Regulatory Documentation Specialist in northern at Unknown Company
This position is listed as full time and able to be worked remotely.