Senior Clinical Research Associate

📋 Description

• Monitor and own the progress of clinical studies at investigative sites
• Ensure clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all
• Coordinate all necessary activities to set up and monitor a study (e.g., identify investigators
• Handle appropriately sized clinical trials and support clinical study teams with larger 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
• Experience monitoring clinical trials across a variety of therapeutic areas
• Availability for domestic travel including overnight stays, up to approximately 50-60% travel
• Fluency in English and the local language

🎁 Benefits

• Empowered to make an impact
• Build meaningful client relationships
• Grow career in an environment that values quality, accountability, and professional development
• Home-based within France