Clinical Database Programmer

Sci Pro are partnering with a growing independent pharmaceutical company who are seeking a Clinical Programmer to support the transition from paper-based data collection to electronic systems across their clinical studies.

This role will take ownership of building and maintaining EDC databases, ensuring high-quality, compliant clinical data, and supporting the implementation and day-to-day management of key clinical systems.

Key Responsibilities

• Build and maintain EDC study databases and eCRFs, including edit checks, UAT, and database go-live
• Support data cleaning, validation, QC, and reporting
• Manage data transfers with external vendors
• Support implementation and maintenance of EDC, eTMF, and CTMS
• Ensure compliance with GCP, GDPR, and data standards (e.g. CDISC/SDTM)
• Act as a key database contact for clinical and project teams

Experience Required

• Experience building EDC databases and programming edit checks
• Background working with clinical study data
• Experience with data/programming tools (e.g. SAS, SPSS, or similar)
• Strong attention to detail and collaborative mindset

If you d like to play a hands-on role in shaping clinical data systems within a growing organisation, we d love to hear from you.