Senior Clinical Research Associate

📋 Description

• Oversee and monitor clinical trial sites to ensure quality, compliance, and patient safety.
• Serve as primary Sponsor point of contact for investigative sites and connect stakeholders.
• Train and align site staff and investigators on trial goals, protocol, and patient treatment
• Conduct site evaluations, training, and on-site/off-site monitoring per GCP/ICH and AbbVie SOPs.
• Engage in risk assessment, site management, and regulatory/quality assurance activities to drive

🎯 Requirements

• Tertiary qualification in health-related disciplines (preferred).
• Minimum 3 years clinically related experience; 2+ years in independent clinical monitoring.
• Familiar with risk-based monitoring, onsite/offsite monitoring, and early phase studies desirable.
• Strong knowledge of regulatory ICH/GCP guidelines and local requirements.
• Excellent communication and cross-functional collaboration skills, with strong planning and

🎁 Benefits

• Global, inclusive workplace with flexible work practices.
• Opportunities to work with a world-class clinical development team.
• Commitment to integrity, ethics, and employee development.