Build and configure the EDC system per data standards (CDASH), study protocol, and eCRF templates
Manage randomisation, ePRO licensing/validation/translation, IMP management
Handle targeted SDV and any additional EDC functionality
Produce study-level EDC documentation (specifications, test plans, training materials)
Apply changes post-live under Change Control

🎯 Requirements

Zelta v2.0 experience essential
Graduate/bachelor’s in Life Sciences or related field
Experience in EDC system creation and Edit Check programming
Strong communication, team orientation, and self-motivation
Proficiency in CDASH and SDTM data standards; CDASH Certification preferred

🎁 Benefits

Opportunity to work across European locations
Collaborative, values-driven culture
Growth and meaningful impact on patient outcomes

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