Clinical Database Programmer

Overview

Support the development, testing and maintenance of Electronic Data Capture (EDC) systems used in clinical trials, primarily using Medidata Rave.

What you'll do

• Design, build, test and maintain clinical study databases within EDC systems.
• Develop and configure eCRFs, edit checks and study-specific database requirements.
• Support clinical data transfers, integrations and database validation activities.
• Troubleshoot technical issues and provide ongoing EDC study support.
• Collaborate with Data Management, project teams and sponsors to ensure successful study delivery.
• Contribute to process improvements, automation and innovative solutions, including the use of AI.
• Support multiple clinical studies and progressively take ownership of study builds.
• Ensure database documentation, quality standards and study timelines are maintained.

What you'll need

• Degree or diploma in Computer Science, Information Technology or a related field, or equivalent relevant experience.
• Previous experience in clinical database development, EDC programming or clinical study builds.
• Previous experience within a CRO or pharmaceutical environment.
• Knowledge of eCRFs, edit checks, database testing and clinical data management processes.
• Understanding of programming principles, logic and database development.
• Strong analytical, problem-solving and organisational skills.
• Experience supporting EDC integrations, technical initiatives or bid defence activities.
• Proactive team player with excellent communication skills and a continuous improvement mindset.

Nice to have

• Hands-on experience with Medidata Rave, including study builds and configuration.
• Knowledge of C# programming and development of custom functions within Medidata Rave.
• Experience with AI tools, automation or AI-assisted programming to improve study development and efficiency.