Senior CRA in Bangalore, भारत

ICON seeks a Senior Clinical Research Associate to oversee clinical trial monitoring and site management in India. The role requires ensuring protocol adherence, regulatory compliance, and data integrity while leading a team of clinical research professionals across multiple trial sites.

Responsibilities

• Monitor clinical trial sites for adherence to protocols, regulatory requirements, and GCP standards
• Conduct site visits to assess performance, identify issues, and provide operational support
• Collaborate with cross-functional teams on timely data collection and accurate reporting
• Train and guide site staff and other CRAs on clinical trial conduct standards
• Build and maintain effective relationships with site personnel and stakeholders

Requirements

• Bachelor's degree in relevant scientific or healthcare field
• Minimum 6 years experience as Clinical Research Associate in onsite monitoring
• Demonstrated experience with oncology trials
• Strong knowledge of clinical trial processes and regulatory requirements including GCP standards
• Proficiency with clinical trial software and monitoring tools
• Ability to manage multiple sites and projects with strong organizational skills
• Willingness to travel approximately 60% as required