Senior Clinical Research Associate

📋 Description

• Monitor and own the progress of clinical studies at investigative sites
• Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and
• Coordinate all necessary activities required to set up and monitor a study (i.e., identify
• Handle appropriately sized clinical trials and support clinical study teams with larger scope trials
• Train and mentor junior staff members
• Interact directly with clients, initiate payments, and participate in proposal activities including

🎯 Requirements

• 4-year college degree or equivalent experience
• Holder of CRA certificate
• Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical
• Extensive experience in IVD (In Vitro Diagnostics), oncology, infectious diseases and
• Proven experience monitoring studies across multiple European countries, ideally including Germany
• Availability for domestic travel including overnight stays, up to approximately 50-60% travel

🎁 Benefits

• Quality, accountability, and professional development
• Empowered to make an impact
• Build meaningful client relationships
• Grow careers in an environment that values quality
• Combines agility and collaboration of a specialized CRO with scientific expertise