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Freelance Study Nurse – Study Coordinator for Digital RCTs

Sobre a vaga

• Conduct study-related visits via video or telephone
• Support and guide the digital informed consent process
• Serve as a point of contact for study participants regarding non-medical questions, as needed
• Support the documentation of study-related information
• Coordinate closely with the study and project teams
• Provide support to study participants and assist with study-related visits in a remote setting

• Experience as a Study Nurse, Study Coordinator, or Clinical Research Nurse
• Experience in clinical trials, ideally randomized controlled trials (RCTs)
• GCP certification
• Excellent communication skills and a friendly manner when interacting with study participants
• Structured, independent approach to work
• Strong digital affinity and ideally experience with remote studies or telemedicine
• Very good German language skills
• Please include your CV, availability, and hourly rate with your application

• Fully remote work
• 6-month contract
• 15 hours per week