Clinical Data Programmer-II

The Clinical Data Programmer-II is responsible for programming activities on clinical trial projects, including designing and implementing clinical databases, programming data review listings, and ensuring compliance with Good Clinical Data Management Practices. The role involves collaborating with project teams, managing external data loads, and supporting the validation of electronic systems in accordance with regulatory requirements. This position requires a graduate in information or life sciences with at least two years of experience in a similar role within a CRO or pharmaceutical company.