📋 Description

• Build EDC system structure, workflow, edit checks and user roles
• Manage randomisation, ePRO licensing/validation/translation
• Handle IMP management and targeted Source Data Verification
• Develop study-level EDC docs and post-live changes
• Follow Change Control for updates to EDC and reporting tools

🎯 Requirements

• Zelta v2.0 experience is essential
• Bachelor’s in Life Sciences or related field
• Experience in EDC system creation and edit check programming
• Strong communication and team collaboration
• Self-motivation and ability to work independently
• CDASH and SDTM data standards knowledge; CDASH certification preferred

🎁 Benefits

• European location flexibility; position available in European locations
• Collaborative, diverse global team in pharma and CRO context