Senior Clinical Research Associate

📋 Description

• Act as primary Sponsor contact for investigative sites and trials.
• Align/train site staff and PI on trial goals and patient care.
• Conduct site evaluation, training, monitoring and closure per GCP/ICH/SOPs.
• Develop site engagement strategy and report progress/impact.
• Ensure data quality and timely safety reporting; support patient recruitment.
• Mentor CRAs and participate in global/local initiatives and risk monitoring.

🎯 Requirements

• Degree in health-related disciplines (e.g., Medical, Scientific, Pharmacy, Nursing).
• Minimum 3 years' clinically related experience; 2+ in independent clinical research monitoring.
• Knowledge of ICH/GCP and applicable regulatory requirements.
• Excellent communication and cross-functional collaboration.
• Strong planning, organizational skills; able to manage multiple projects.
• Proficient with tools to support site activities and data quality.