Principal Database Programmer

Overview

Principal Database Programmer responsible for managing database programming across clinical studies from start to post database lock, ensuring development, support, maintenance, and regulatory compliance.

What you'll do

• Manage programming aspects of clinical databases and applications from study start to post database lock.
• Develop, test, and validate programs and clinical databases for client-related projects and third-party applications.
• Provide system administration and advanced technical support for internal applications, clinical databases, and related projects.
• Troubleshoot and resolve software and clinical database problems.
• Lead operational study/program teams and provide operational and technical training to end users and junior staff.
• Provide planning estimates (scope, schedule/timelines, forecasting, and resource requirements) and support project budgeting and forecasting.

What you'll need

• Minimum 8 years’ experience.
• Strong experience in Oncology; autoimmune experience is noted as an advantage.
• Strong experience with Rave and Veeva.
• Proficiency with CDISC standards (CDASH, SDTM, ADaM).
• Proficiency in clinical database management system development.
• Experience in object-oriented programming (e.g., C#, C++, VBS).
• Professional English communication (written and oral).

• Autoimmune experience is described as a strong advantage.
• Experience in utilizing various database programming systems is listed as a preferred item (optional).
• Experience in a clinical/scientific/healthcare discipline and multiple therapeutic areas is listed as preferred (optional).

Details

• Full-time, permanent role.
• Can be covered fully remotely from European locations.
• Location: Remote, Hungary.