Sr. Clinical Research Associate (Germany)

📋 Description Onsite/remote site monitoring per SOPs and ICH-GCP Coordinate data review against source documents Manage data queries and issue escalation Ship clinical supplies and study docs Train site staff on protocol, systems and study docs Attend study progress meetings and Investigator meetings 🎯 Requirements College diploma/degree required 4-6 years related experience Strong communication and attention to detail Critical thinking and collaboration skills Willingness to travel 5–8+ days per month 🎁 Benefits Home-based with regular travel Mentoring CRA I/II and process improvements