Senior Clinical Research Associate

📋 Description

• Oversee and monitor clinical trial sites ensuring quality and patient safety.
• Serve as sponsor point of contact for investigative sites.
• Train and engage site staff and investigators on trial goals and protocols.
• Conduct site evaluations, monitoring, and closures per GCP/ICH and AbbVie SOPs.
• Collaborate with Central Monitoring to detect study risks early.
• Support compliant trial execution and patient recruitment plans.

🎯 Requirements

• Health-related tertiary qualification preferred.
• 3+ years clinically related experience, incl. site monitoring.
• Knowledge of ICH/GCP, regulatory requirements, and risk-based monitoring.
• Strong communication and cross-functional collaboration skills.
• Ability to plan, organize, and manage multiple projects.
• Proficiency with site engagement tools and data reporting.

🎁 Benefits

• Equitable, inclusive workplace with flexible, global collaboration.
• Code of Conduct and business integrity programs.
• Global opportunities within AbbVie’s R&D network.