Senior Clinical Research Associate

📋 Description

• Ensure protocol-level execution of SMM deliverables for assigned sites/studies
• Maintain clinical trial management systems and ensure timely payments
• Ensure adherence to GCP, ICH Guidelines, and regulatory requirements
• Prepare and follow up on site audits/inspections, contribute to CAPAs
• Coach and mentor CRAs, provide input into their development
• Manage remote data review per IDRP and Monitoring Plan

🎯 Requirements

• Bachelor's degree or equivalent, health-related preferred
• Minimum 5 years site monitoring experience
• Strong analytical and critical thinking skills
• Excellent interpersonal and communication skills
• Strong planning and organizational skills
• Demonstrated business ethics and integrity