Clinical Research Associate II

📋 Description

• Monitor and own progress of clinical studies at sites per protocol and regs.
• Coordinate site setup tasks: investigator identification, regulatory prep, pre-study visits.
• Ensure studies are conducted, recorded, and reported per ICH-GCP and SOPs.
• Support growth through ongoing study oversight and issue resolution.
• Travel up to 50-60% for domestic sites as needed.
• Role based in Madrid or Barcelona, Spain; remote work option.

🎯 Requirements

• 4-year college degree or equivalent experience
• 2+ years as a CRA in CRO or pharma/biotech
• Site management or equivalent clinical research experience
• Oncology monitoring experience
• Fluency in English; local language for country of posting
• Candidates must reside in Madrid or Barcelona

🎁 Benefits

• Flexible work-life balance in a smaller CRO
• Direct line management support and influence on projects