Clinical Trials Assistant

A company is looking for a Clinical Trials Assistant (CTA) to support Clinical Operations in completing studies in compliance with regulations.

Key Responsibilities

Assist in the preparation and management of regulatory documents and study-related materials

Monitor and track clinical trial progress, including status updates and data reviews

Act as a central contact for project communications and documentation

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; CTA experience preferred but not required

Demonstrated organizational and coordination skills

Solid understanding of clinical drug development preferred