Clinical Trial Assistant

As a Clinical Trial Assistant, you will support our clinical research teams in the planning, execution, and management of clinical trials. Your responsibilities will include: 

•  Assisting with the preparation and organization of trial documentation. 
• Maintaining accurate and up-to-date study files and records. 
• Coordinating communications between study sites, investigators, and internal teams. 
• Supporting the management of trial supplies and logistics. 
• Contributing to regulatory compliance and quality assurance activities. 

 CTA roles present an excellent opportunity for individuals who are eager to contribute to groundbreaking research.

At ICON, we believe in nurturing talent and providing our employees with pathways for professional development. As a Clinical Trial Assistant, you will have: 

• Career Progression: Gain the skills and experience necessary to advance to roles such as Clinical Research Associate (CRA), Project Manager, or other specialized positions within clinical operations. 
• Training and Development: Access to continuous training programs and mentorship opportunities to enhance your knowledge of clinical research processes and regulatory requirements. 
• Global Exposure: Work with diverse teams across various therapeutic areas, gaining valuable insights and experience in international clinical trials.

The role of a Clinical Trial Assistant is vital to the success of clinical research. By ensuring that trials run smoothly and efficiently, you directly contribute to: 

• Patient Safety: Supporting the meticulous organization of trial data and adherence to protocols ensures the highest standards of patient care and safety. 
• Innovative Treatments: Your work helps facilitate the development of new medications and therapies that can change the lives of patients around the world. 
• Advancing Science: Be part of a team that pushes the boundaries of medical science, participating in studies that may lead to significant breakthroughs in treatment options.