Senior Clinical Research Associate

📋 Description

• Oversee and monitor clinical trial sites to ensure quality, compliance, and patient safety.
• Act as primary sponsor point of contact for investigative sites, connecting stakeholders.
• Train and motivate site staff and investigators on trial goals, protocols, and patient treatment
• Conduct site evaluation, training, monitoring, and site closure with adherence to GCPs and AbbVie
• Identify and engage investigators/sites to support planned studies with qualified investigators.
• Ensure data quality and timely reporting, including safety events and regulatory readiness.

🎯 Requirements

• Appropriate tertiary qualification in health-related disciplines (preferred).
• Minimum 3 years clinically related experience; 2 years in independent clinical research monitoring.
• Experience in Early Phase 1 and First-in-Human studies desirable.
• Strong knowledge of regulatory requirements, ICH/GCP, and applicable policies.
• Excellent communication and cross-functional collaboration skills.
• Ability to plan, organize, and manage multiple projects in a dynamic environment.

🎁 Benefits

• AbbVie equal opportunity workplace with inclusive culture.
• Global collaboration in a matrix environment; flexible and supportive policies.