Clinical Research Associate

Description

• Manage study sites to ensure compliance with protocols, regulations, and Novartis procedures
• Conduct site initiation visits and deliver tailored training to site personnel
• Perform ongoing site monitoring to ensure data quality and patient safety
• Implement site management strategies to address compliance and operational issues
• Maintain accurate and timely documentation of all monitoring activities
• Ensure continuous updates to global and local electronic systems
• Identify, resolve, and escalate site-related issues as appropriate
• Maintain up-to-date Trial Master Files and collect essential site documents
• Support audit and inspection readiness, ensuring timely corrective actions
• Collaborate with internal teams to support recruitment and contingency planning

Qualifications

• Degree in a scientific or health-related discipline; advanced degree preferred
• Fluent in written and spoken English
• Up to two years of experience in clinical research, with focus on monitoring and trial execution
• Strong knowledge of international standards including GCP and ICH
• Proven ability to manage sites independently and resolve issues proactively
• Willingness and ability to travel domestically and internationally as needed
• Full UK driving license