Clinical Database Programmer

SciPro 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