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 Project Managers with trials that are
• Train and mentor junior staff members
• Interact directly with clients, initiate payments, and participate in proposal activities

🎯 Requirements

• 4-year college degree or equivalent experience
• 3+ years of independent monitoring experience within the CRO or pharmaceutical industry
• Experience managing oncology studies
• Availability for domestic travel including overnight stays, which may constitute up to
• Fluency in Polish and English

🎁 Benefits

• Focus on an average of one to two studies setting you up to be a protocol expert
• Reasonable travel and work/life balance
• Influence and impact with direct line management support
• Amazing people and enjoyable quality of life