Clinical Research Associate II

📋 Description

• Monitor and own progress of clinical studies at sites per protocol and ICH-GCP.
• Coordinate study setup and ongoing monitoring activities.
• Travel up to 50-60% with a smaller CRO and close management support.
• Ensure quality data and compliant reporting per SOPs and regulations.

🎯 Requirements

• 4-year college degree or equivalent.
• 2+ years as a CRA in CRO/pharma/biotech.
• Site management or equivalent clinical research experience.
• Oncology monitoring experience.
• Residency in Madrid or Barcelona; fluent English and local language.
• Availability for domestic travel up to 50-60%.

🎁 Benefits

• Strong work-life balance and supportive management.
• Voice heard; influence project outcomes.
• Path to protocol expert with fewer protocols.
• Reasonable travel expectations.