Digital Research Access Manager

o Lead and coordinate a key digital workstream, ensuring seamless delivery across regional partners o Shape and optimise processes by integrating digital tools, streamlining workflows and coordinating multi-stakeholder collaborations to speed up trial setup, improve recruitment, and enhance efficiency Realise the potential of digital data to widen patient access to research, helping to achieve the UK Clinical Research Delivery 'Right Research Right Setting' ambition.o Oversee governance, reporting, and performance of a workstream supporting participant identification and recruitment in healthcare across Sussex, ensuring compliance with regulatory and data protection requirements.o Build collaborations with all the digital and data infrastructure in the diverse partnerships across Sussex, to ensure the right tools are used to support the right study

• Compliment the CRDCs other workstreams to ensure we meet the government's150 day research set up targets

The Commercial Research Delivery Centre Sussex is reimagining the way commercial clinical trials are set up and delivered, working across Sussex to ensure wider access to research for our whole community. Building on the infrastructure, support, and expertise already in place across the region, CRDC Sussex is bringing together system partners to accelerate clinical trial set up and delivery, while working closely with our public stakeholders to widen our reach to people that haven't previously had access to commercial research. The Sussex CRDC is not just another piece of research infrastructure; we are implementing processes that are shaping the future of commercial research in Sussex. As our Digital Research Access Manager you'll sit at the heart of this transformation. You'll be responsible for accelerating research processes by integrating digital tools and streamlining workflows. You will manage coordination between multiple partners, (including NHS Trusts, General Practices, care homes, community pharmacy, and beyond), working with leading pharmaceutical companies and cutting-edge research centres, to make commercial clinical trials faster, smarter, and available to more people. Currently research delivery depends substantially on accessing data about potential participants on a clinician-by-clinician basis.