Required Skills BSc in Biomedical Health or Life Sciences Clinical Trial Management Phase I - IV trials experience Job Summary We are seeking an experienced Clinical Trials Manager to join our Clinical and Application Research team. In this role, you will be responsible for managing all aspects of clinical trials, from designing trial documentation and regulatory submissions to overseeing trial progress and data management. You will coordinate a multi-site team to ensure trials are conducted according to regulatory and ethical standards, delivered on time, and within budget. Key Responsibilities: Design and manage clinical trials, author trial documentation, and handle regulatory submissions. Lead data collection, statistical analysis, and reporting. Ensure trials meet ICH-GCP guidelines and other industry regulations. Oversee trial sites and manage trial personnel. Experience Proven experience in clinical trial management, with knowledge of ICH-GCP and EU Medical Device regulations. Experience in Phase I-IV trials: Phase II - III is preferred Job Responsibilities Design and manage clinical trials, author trial documentation, and handle regulatory submissions. Lead data collection, statistical analysis, and reporting. Ensure trials meet ICH-GCP guidelines and other industry regulations. Oversee trial sites and manage trial personnel.