Senior Clinical Research Associate

📋 Description Study management: Responsibility for a selection of studies, from site selection through conduct to Coordination: Close collaboration with local CRA colleagues in various study teams, contributing to Monitoring: Oversight of a selection of investigator sites and monitoring of collaboration with Compliance: Ensuring that all internal and external requirements are met in your projects and that 🎯 Requirements Bachelor's degree or equivalent, ideally in a health-related field (e.g., medicine, natural At least 3 years of on-site and remote monitoring experience in clinical studies of phases 1-4, as Planning skills, excellent organizational talent, analytical thinking, independent and structured Excellent social skills, enthusiasm, self-reflection, flexibility, and persuasion. Fluent German and English language skills. 🎁 Benefits Appropriate remuneration: attractive salary plus comprehensive social benefits. Quick start: intensive onboarding including a dedicated buddy. Flexible work: modern working models for a healthy work-life balance. Achieving more together: in a diverse, open working environment and a unique culture where everyone Staying healthy: strong health management with diverse prevention, exercise, and well-being offers. Growth without limits: diverse career and development opportunities in an international