You will oversee the development, maintenance, and compliance of database builds and (EDC) standards to support clinical studies. This includes tasks such as creating Edit Checks, (CFR) modules, and standard/custom reports. You will also serve as a resource for addressing database issues and providing problem-solving support related to clinical database technology, capabilities, and functionality. Identifying process deficiencies and suggesting improvements to optimise clinical programming processes will be another key aspect of your role. Additionally, you will contribute to the hiring, training, and evaluation of Clinical Database Programmers. Your involvement will extend to participating in the development of departmental SOPs and other relevant controlled documents. Furthermore, you will have the opportunity to participate in business development meetings and activities as requested.