Clinical Trial Associate

Job description

Clinical Trial Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: Your role will involve delivering clinical research work to a high standard, working closely with your team and stakeholders. Key responsibilities include: - Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements. - Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions. - Support the preparation of study-related materials, such as informed consent forms and case report forms. - Work with cross-functional teams to facilitate communication and ensure smooth trial ex...