Senior Clinical Research Associate

📋 Description

• Oversee and monitor clinical trial sites to ensure quality, compliance, and patient safety.
• Act as primary sponsor point of contact for investigative sites and align stakeholders.
• Provide site staff training and maintain trusted partnerships with investigators.
• Conduct site evaluations, monitoring, and site closure activities per regulations and SOPs.
• Engage sites with tailored strategies, report progress, and report study impact.
• Support recruitment/retention strategies and ensure protocol compliance and data integrity.

🎯 Requirements

• Appropriate tertiary qualification in health related disciplines (e.g., Medical, Scientific
• Minimum 3 years clinically related experience, with 2 years in independent clinical research
• Familiar with risk-based monitoring, onsite and offsite monitoring.
• Strong knowledge of regulatory and ICH/GCP guidelines and local policies.
• Excellent communication and cross-functional collaboration skills.
• Strong planning, organization, and ability to manage multiple priorities.

🎁 Benefits