• Define trial-specific data management procedures, including the Data Management Plan and Data Validation Plan.
• Coordinate development, administration, updates, and UAT of eCRF and eDiary/eCOA systems, including user management
• Organize and specify electronic data transfers from external data sources
• Define and manage regular data management status reports, including content and distribution
• Oversee medical coding activities (MedDRA, WHO-DD) and ensure accurate safety data reconciliation
• Coordinate database freeze and lock activities, ensuring timelines and data quality standards are met
• Drive process optimization and oversee CRO performance, ensuring compliance, quality, and cross-functional collaboration

• Master’s degree in a relevant field (e.g., Medical Documentation, Informatics, Bioinformatics, Natural Sciences) with 3+ years of clinical data management experience
• Proficiency in Microsoft Office, EDC systems, and SAS; knowledge of CDISC and ISO 14155 is a plus
• Strong understanding of ICH, GCP, and FDA guidelines and their practical application
• Analytical, structured, and solution-oriented working style with strong organizational and project management skills
• High resilience, emotional intelligence, and ability to adapt quickly to changing priorities
• Strong team player with cross-functional collaboration skills and ability to influence others
• Fluent in English with excellent written, verbal, and interpersonal communication skills

• Experience in exciting and international projects
• Continuous salary development
• Da Vinci Corporate Benefits
• On-the-job training and language courses
• Appreciation, motivation and commitment

Nothing provides more motivation than success. Da Vinci Engineering is highly committed to ensuring the own employees' success. Become a part of us!