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Senior Clinical Database Programmer will work under the supervision of Principal CDP (or higher-level role) but may work independently as project lead. Working closely with members of Data Management, Statistics, Information Technology (IT), and Quality Control (QC) Departments, this role is responsible for the design and development of electronic and paper Case Report Forms and for managing, directing, and enabling the setup of studies using the Company’s clinical data management systems. The position includes the maintenance and development of computer programs and processes that support the team’s activities, within scope, budget, and timelines in compliance with the United Kingdom Statutory Instrument 2004 No. 1031, its subsequent amendments, ICH guidelines for Good Clinical Practice, and other national and international standards and legislation, Company procedures, and client instructions.