Clinical Research Associate or SrCRA(m/w/x)

Anforderungen

• University degree in life science or other scientific discipline or apprenticeship in health care field
• Minimum of two years of on-site monitoring experience or equivalent combination of education, training, and experience
• Knowledge of clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Strong written and verbal communication skills, attention to detail, and ability to work in a fast-paced environment
• Fluent verbal and written language skills in German and English (C1 level) plus good verbal demand in French and Italian
• Flexibility to travel up to 40-60% of working time
• Driver’s license class B

Aufgaben

• Perform site selection and initiation visits
• Conduct monitoring and close-out visits
• Support the development of subject recruitment plans
• Evaluate site practices for quality and regulatory compliance
• Track regulatory submissions and recruitment progress
• Ensure case report form (CRF) completion and resolve data queries
• Collaborate with study site experts and client representatives
• Engage in remote monitoring and study start-up processes as needed
• Mentor less experienced team members and provide subject matter expertise

Berufserfahrung

Ausbildung

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