Job Title: Analyst - Regulatory Information Management Location: Marlow Contract: 12 Months / Hybrid 3 days onsite Hours: 37.5 hours per weekRates: 23 p/h Job DescriptionSRG are looking for an analyst - regulatory information management for a leading pharmaceutical company based in Marlow. As part of this role, you will be supporting process improvement initiatives. Support structured data submissions and all related tasks, including xEVMPD, SPOR and IDMP implementation.Support Regulatory Information Management (RIM) globally, focusing on key systems and processes, including COSMOS (RIM system) Supports Data enrichment and archiving remediation initiatives.Work with members of the Regulatory Lifecycle Management team to share knowledge and improve RIM processes.Build and maintains relationships with Regulatory and other staff within and outside of the region to ensure effective communication and efficient implementation of regulatory information management. Duties and Responsibilities Subject to internal QC audit, ensure all data submissions and related reference/master data are managed accurately and in accordance with SOPs.Establish relationships with ''in-country'' teams and global regulatory teams to ensure that they are aware of how data submissions are managed.Maintain awareness of International regulatory procedures and how any changes may impact reference and master data management within the Regulatory Information Management system.Work with other Local System ..... full job details .....