Senior Clinical Research Associate

📋 Description

• Oversee and monitor clinical trial sites to ensure quality, compliance, and patient safety.
• Act as sponsor point of contact for investigative sites and connect stakeholders.
• Conduct site evaluation, training, monitoring, and site closure with GCP/ICH adherence.
• Guide site staff and investigators on protocol and patient treatment principles.
• Monitor risk signals and collaborate with Central Monitoring to detect study issues.
• Ensure data quality, timely safety reporting, and regulatory readiness.

🎯 Requirements

• Teritary qualification in health-related disciplines preferred.
• Minimum 3 years clinically related experience; 2 years in independent monitoring.
• Strong knowledge of ICH/GCP, regulatory requirements, and safety reporting.
• Excellent communication and cross-functional collaboration skills.
• Strong planning, organization, and site relationship skills.
• Ability to use technology/tools to support site-focused performance.

🎁 Benefits

• Competitive compensation and benefits package.
• Opportunity to work in a global, matrixed environment.
• Flexible, inclusive work culture with a focus on patient impact.