Evolution Research Group
The CTA supports Clinical Operations by managing the trial master file, regulatory documents, and study communications to ensure compliance with FDA and GCP guidelines. Responsibilities include tracking trial progress, coordinating project meetings, and assisting with study drug release.
Requires a minimum of 2 years of clinical research experience and a high school diploma, though a bachelor's degree is preferred. Candidates must have a strong knowledge of GCP and ICH guidelines and proficiency in Microsoft Office.
Job Title: Clinical Trials Assistant (CTA)
Location: Remote
The Clinical Trials Assistant supports Clinical Operations to ensure studies are completed, on time, within budget and in compliance with SOPs, FDA regulations and ICH/GCP guidelines. The CTA will archive and organize clinical trial master file documents, including clinical study site documents, generate filing indexes and maintain currents lists of correspondence.
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