Clinical Research Associate II

📋 Description

• Monitor clinical studies at sites to ensure protocol, SOPs, and ICH-GCP compliance.
• Coordinate study setup: identify investigators, regulatory submissions, and initiation visits.
• Travel domestically up to 50-60%; international travel may be required for some roles.
• Work in a smaller CRO with close management and influence on trial delivery.
• Join a team focused on Oncology and Rare Disease with opportunities to impact patients.

🎯 Requirements

• Life science degree and/or equivalent experience.
• 2+ years as CRA in CRO or pharma; site management experience.
• Availability for domestic travel up to 50-60%; international travel may be required for some senior positions.
• Fluency in English and Hungarian.
• Oncology monitoring experience is a plus.
• Study start-up activities experience.

🎁 Benefits

• Remote position with travel to sites for monitoring visits.
• Reasonable travel and strong work-life balance.
• Opportunity to influence trial delivery in a smaller CRO with direct management support.
• Focus on Oncology and Rare Disease in a collaborative environment.