We are seeking a Data Manager to focus on Real World Data for Early Access projects. This role involves partnering with clients and internal stakeholders to provide practical support and implement real-world data collection projects within the early access/named patient/compassionate use setting. Responsibilities Act as the main point of contact for clients regarding real-world data. Lead the scoping and delivery of real-world data projects. Participate in proposal development and project kick-off meetings to guide and define data collection strategies. Provide oversight of all data management activities, including project design, set-up, and implementation. Develop core project documents for data management, such as Data Management Plans (DMPs), Data Validation Plans (DVPs), and Case Report Form (CRF) completion guidelines. Work closely with the Technical Operations team to design data collection solutions that meet individual client requirements. Lead the design and validation of CRF specifications and edit checks for electronic data capture (EDC) systems. Create and test study databases according to client specifications. Partner with EDC vendors to ensure data projects are built on time and accurately reflect client requirements. Monitor and review all data submitted via internal and external platforms to support real-world data projects. Ensure real-time data management and maintain overall data quality and completeness. Conduct data reviews, identify data issues, and generate queries as needed. Undertake data cleansing and descriptive data analysis at agreed frequencies with clients. Provide expert insight into developing and enhancing real-world data offerings. Qualifications Previous experience working as a data manager with Clinical trial / Real World Data experience is essential Strong proficiency with EDC platforms for clinical data collection. Deep understanding of data management processes and standards. Experience attending client calls and being comfortable being client facing Experience in analysing and processing clinical study data. Experience in working with international organizations and multicultural environments. Proactive team player with excellent communication skills. Ideally you will be able to commute to Slough area to attend the office on a hybrid basis however if you are further away then remote could be open to consideration.