Clinical Research Associate II

📋 Description

• Acts as primary point of contact for investigative sites, providing contextual information on
• Aligns, trains, and motivates site staff and principal investigators on clinical trial goals
• Conducts site evaluation, training, routine monitoring, and site closure activities in compliance
• Develops and customizes site engagement strategies, gathers local insights, and uses CRM tools to
• Connects study protocols and scientific principles to day-to-day trial execution, ensuring
• Mentors and trains less experienced CRAs; participates in global/local task forces as assigned.

🎯 Requirements

• Appropriate tertiary qualification in health-related disciplines (Medical, Scientific, Nursing)
• Minimum 1 year of clinically related experience, including 6 months in clinical research monitoring
• Familiarity with risk-based monitoring approach, onsite and offsite monitoring.
• Knowledge of relevant therapeutic area indications preferred.
• Advanced knowledge of local regulatory requirements, ICH/GCP guidelines, and applicable policies.
• Strong cross-functional collaboration skills.