Senior Clinical Research Associate

📋 Description

• Oversee and monitor clinical trial sites to ensure quality, compliance, and patient safety.
• Collaborate with Sponsors, site staff, and investigators to advance trial execution.
• Train and motivate site staff on trial goals, protocols, and patient treatment principles.
• Conduct site evaluations, monitoring, and closure activities per SOPs and GCP/ICH.
• Report adverse events within 24 hours; participate in risk assessment and issue mitigation.
• Maintain data quality and ensure timely reporting of safety and study data.

🎯 Requirements

• Tertiary qualification in health-related field preferred.
• Minimum 3 years clinically related experience; experience in monitoring trials is preferred.
• Strong knowledge of ICH/GCP, regulatory requirements, and site engagement strategies.
• Excellent communication, collaboration, planning, and organizational skills.
• Ability to leverage technology to support site-centric trial delivery.
• Ability to work in a fast-paced, global environment with multiple projects.

🎁 Benefits

• Equal opportunity employer and inclusive workplace.
• Flexible collaboration in an international, matrixed team.