Clinical Research Associate II

📋 Description

• Primary point of contact for investigative sites; provides contextual information on clinical
• Aligns, trains, and motivates site staff and principal investigator on clinical trial goals
• Conducts site evaluation, training, routine, and closure monitoring activities in compliance with
• Develops and customizes site engagement strategies using CRM tools to track progress and measure
• Connects study protocol, scientific principles, and clinical trial requirements to day-to-day
• Mentors and trains less experienced CRAs; may participate in global/local task forces.

🎯 Requirements

• Appropriate tertiary qualification in health-related disciplines (Medical, Scientific, Nursing)
• Minimum 1 year clinically related experience, including 6 months in clinical research monitoring of
• Knowledge of therapeutic area indications preferred; ability to understand and apply scientific
• Advanced knowledge of local regulatory requirements, ICH/GCP guidelines, and applicable policies.
• Strong cross-functional collaboration skills.
• Strong planning and organizational skills; ability to work in dynamic environment with competing