Clinical Programmer

About the role

The Clinical Programmer will design, develop, test, and maintain clinical databases and technology systems, ensuring data quality and regulatory compliance across studies. This role collaborates closely with cross‑functional teams to translate business needs into technical solutions.

Key responsibilities

• Build, integrate, and maintain clinical databases, edit checks, reporting, and user testing while supporting governance of cross‑study programming environments.
• Design, develop, test, and maintain clinical technology systems (EDC, RTSM, eCOA/ePRO) using programming and automation frameworks.
• Implement and validate complex data logic such as edit checks, derivations, and dynamic rules.
• Develop advanced reporting solutions, dashboards, and visual analytics using enterprise platforms.
• Configure, test, and validate data sources for integrations and transformations across systems.
• Lead UAT activities, translate requirements into technical specifications, and refine reporting standards.

Required profile

• B.A. or B.S. degree, preferably in Biotechnology; candidates from Computer Science or related fields are also considered.
• Minimum of 3 years experience in clinical data programming, data engineering, or related clinical operations functions.
• Strong understanding of clinical data flow, regulatory standards, GCP, and audit‑ready documentation.

Required skills

• Proficiency in SQL, Python, SAS, and R for data collection, integration, transformation, and reporting.
• Experience with data‑management tools and platforms, scripting and automating data ingestion, cleaning, and reporting processes.
• Knowledge of SDLC, validation practices, change control, and release management.
• English proficiency at B2+ level.