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
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