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,vivience, 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 love2264 to hear from you

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