Clinical Data EDC Consultant – Rave (m/f/d)

We are currently looking for an experienced Rave EDC Consultant (m/f/d) to support an international Life Sciences project in the setup and optimization of clinical data capture systems.

The role focuses on hands‑on work with the Medidata Rave eDC Designer module, including study build, data structure configuration, and implementation of study‑specific logic.

Key Responsibilities

• Design and build studies based on clinical protocols (e.g., SoA, datasets, codelists)
• Adapt and enhance existing global Rave libraries
• Configure data objects, forms, and study components
• Develop and implement edit checks and custom functions (CF)
• Ensure data quality, consistency, and compliance
• Collaborate with cross‑functional teams and support the Rave environment

Requirements

• Hands‑on experience with Medidata Rave EDC (Designer module)
• Strong background in study build / eDC design
• Experience with edit checks and custom functions
• Good understanding of clinical trial processes and CDISC standards
• Independent working style and strong problem‑solving skills
• Fluent in English
• Valid EU or UK work permit

Nice to have

• Experience in international clinical projects
• Knowledge of regulatory requirements in clinical data management