CRA I

📋 Description

• Act as primary contact for investigative sites, sharing trial context and coordinating with AbbVie
• Align and train site staff and principal investigators on trial goals, protocol, and treatment
• Conduct site evaluations, training, monitoring, and site closures per protocol and regulatory
• Customize site engagement strategy using tools like CRM to report progress and measure impact.
• Support recruitment and retention planning based on patient journey and disease area knowledge.
• Monitor risk with Central Monitoring team to ensure study performance and patient safety.

🎯 Requirements

• Appropriate tertiary qualification in health-related fields or equivalent experience.
• Experience in clinical research coordinating or data management preferred.
• Knowledge of therapeutic areas and ICH/GCP guidelines and policies.
• Strong collaboration, planning, and organizational skills in dynamic environments.
• Ability to leverage technology for customer-centric site support and issue resolution.
• Excellent communication and relationship-building skills to foster trusted partnerships.

🎁 Benefits

• Equal opportunity employer information may apply.
• Company information and social links available in the job description.