Clinical Trials Assistant

A company is looking for a Clinical Trials Assistant (CTA) to support Clinical Operations in ensuring studies are completed on time and in compliance with regulations.

Key Responsibilities

Assist in the preparation and management of clinical and regulatory documents

Participate in the planning of investigator meetings and handle study-related communications

Monitor clinical trial progress and maintain trial master files

Required Qualifications

BS / BA preferred; high school diploma or equivalent required

General knowledge of clinical research requirements, including GCP and ICH guidelines

Minimum of 2 years of clinical research experience required

Demonstrated organizational and coordination skills

Solid understanding of clinical drug development preferred