Clinical Trial Associate

Clinical Trial Associate ICON Sofia, Bulgaria 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 execution; Contribute to the tracking and reporting of clinical trial metrics and milestones. Your Profile: You will bring relevant clinical research experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in a scientific or healthcare-related field; Prior experience in clinical research as a CTA or clinical site study coordinator; Previous experience with eTMF systems is an advantage; Ability to prioritize, multitask, and stay organized in a dynamic work environment; Knowledge of clinical trial processes, regulations, and guidelines; Excellent organizational and communication skills; Ability to work collaboratively in a fast-paced environment with attention to detail. Apply Now