Clinical Research Associate

📋 Description

• Hybrid CRA role in Amadora, Portugal
• Partner with investigators and site staff for study delivery
• Ensure quality conduct and patient safety across Phase I–IV
• Coordinate site qualification, initiation, monitoring, and close-out visits
• Train site personnel on protocol and safety reporting
• Oversee risks, CAPA plans, and regulatory compliance

🎯 Requirements

• Bachelor’s degree in health/science or related field preferred
• Minimum one year in clinical research monitoring
• Strong planning, organizational, and communication skills
• Analytical, problem-solving, and ability to manage multiple priorities
• Self-motivated, collaborative, committed to quality and patient safety

🎁 Benefits

• AbbVie culture and values: All4OneAbbVie, Decide Smart & Sure, Agile & Accountable
• Equal Opportunity Employer; focus on integrity, innovation and collaboration
• US & Puerto Rico resources for accommodations and support