CRA II/Sr CRA - Sponsor-Dedicated FSP - Germany (m/f/d)

Exciting opportunity for an experienced Clinical Research Associate to manage clinical trial sites across Germany, ensuring compliance with protocols and regulations. Key responsibilities include site monitoring and collaboration with project teams. Ideal for candidates with strong clinical monitoring skills and at least two years’ independent experience.

Skills

• clinical monitoring
• ich-gcp compliance
• site risk-based monitoring
• regulatory compliance
• sop compliance
• sdr/sdv/crf review
• investigational product accountability
• root cause analysis
• capa
• audit readiness
• inspection readiness
• ctms
• therapeutic area knowledge
• medical terminology
• stakeholder management
• mentoring