, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Trial Administrator... to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design...
efficiency throughout the clinical development process. Monitoring trial progress and performance metrics, providing insights..., offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support...
of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP...CRA / MY / Office-based ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re...
pricing strategies for clinical trial investigators. Your role will involve assessing cost structures, optimizing pricing... strong relationships with investigators. What You Will Be Doing: Analyzing and developing pricing strategies for clinical trial...
, QA & MI. Provide medical and scientific support for clinical development programs, including protocol development, trial...'s registered products across all territories, aligning with global and regional objectives. Lead medical affairs initiatives...
), Change Review Committee (CRC), and local change control procedures. Manage regulatory submissions to support clinical trial... local registration plans in alignment with local business objectives and global regulatory strategy. Monitor the progress...
) Global Study Manager and various CLS departments involved in the clinical protocol Close collaboration with the Global Study... Statement of Work specifications and very good understanding of how they impact every lab services aspect of the clinical trial...
and dynamic team. As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities.... What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical...
. Manage regulatory submissions to support clinical trial activities in the OPU, if applicable. 2. Regulatory Intelligence..., ensuring timely approvals. Develop local registration plans in alignment with local business objectives and global regulatory...