Humaneva Group

General

• Coordination and support of clinical trials while ensuring regulatory and quality requirements are met
• Collaboration with study nurses, principal investigators, pharmacists and study coordinators
• Review and analysis of study protocols, study procedures, examination plans, and inclusion/exclusion criteria
• Creation, maintenance and review of medical forms and study-related documentation
• Documentation, analysis and management of study-related data using MS Office applications
• Work with study-specific IT systems and onboarding to new digital applications and processes
• Communication with international team members and external stakeholders in English
• Structured organization and coordination of relevant processes to ensure smooth study conduct

Digital Start-Up Specialist