Principal Database Programmer

Overview

Principal Database Programmer to manage database programming for clinical databases and applications across study timelines, from study start through post database lock.

What you'll do

• Manage programming aspects of clinical databases and applications from study start to post database lock.
• Lead operational study team/program programming team members on assigned studies.
• Develop, test, and validate programs and clinical databases for client-related projects and third-party applications.
• Provide system administration and advanced technical support for clinical databases and internally developed applications.
• Troubleshoot and resolve software and clinical database problems.
• Build and support study-specific validation documents and support data management from CRF design to post database close/archival.
• Lead planning estimates for scope, schedule/timelines, forecasting, and resource requirements, including budget management.

What you'll need

• Minimum 8 years’ experience.
• Strong experience in Oncology; autoimmune disease experience is described as advantageous.
• Strong experience with Rave and Veeva.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook).
• Experience with Object Oriented Programming (C#, C++, VBS, etc.).
• Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.).
• Proficiency in more than one CDMS system, including building forms, edit checks, and complex rule development.

Details

• Role can be covered fully remotely from European locations.
• Employment: full-time, permanent.
• May require some travel.