We are currently seeking a Clinical Trial Assistant (CTA) to join our diverse and dynamic team. As a CTA at ICON Plc, you will play a key role in supporting the management and execution of clinical trials by handling a range of administrative and operational tasks. You will contribute to the smooth execution of clinical trials through efficient coordination, documentation, and communication with various stakeholders. **What You Will Be Doing:** + Providing administrative support for clinical trials, including managing documentation, coordinating meetings, and maintaining trial-related records. + Assisting in the preparation and submission of regulatory documents and ensuring compliance with study protocols and regulatory requirements. + Collaborating with cross-functional teams to support trial operations and resolve any issues that arise during the course of the study. + Monitoring and tracking trial progress, including managing site communications and ensuring timely delivery of study materials. + Building and maintaining strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support overall project success. **Your Profile:** + Bachelor's degree or certification in a relevant field such as life sciences, healthcare, or clinical research highly preferred. + Extensive experience in a clinical trial support role, with a solid understanding of clinical trial processes and regulatory requirements. + Strong organizational and multitasking skills, with the ability to manage multiple tasks and projects effectively. + Proficiency in clinical trial management systems and relevant software, with a keen eye for detail in documentation and data management. + Excellent communication, interpersonal, and problem-solving skills, with the ability to work collaboratively with diverse teams and stakeholders.