CRA` in Thana, भारत

Clinical Research Associate at IQVIA responsible for site monitoring, protocol compliance, and study data management across assigned clinical trial sites. Ensures adherence to GCP/ICH guidelines and manages site documentation, recruitment, and regulatory requirements.

Responsibilities

• Conduct site monitoring visits including initiation, ongoing monitoring, and closeout activities
• Develop and track subject recruitment plans in coordination with site personnel
• Administer protocol training and maintain regular communication with assigned sites
• Review study data quality and protocol adherence; escalate compliance issues
• Track study progress including regulatory submissions, enrollment, CRF completion, and data queries

Requirements

• Bachelor's degree in scientific or healthcare discipline
• Minimum 1 year of on-site clinical trial monitoring experience
• Strong knowledge of GCP and ICH regulatory guidelines
• Proficiency with Microsoft Office (Word, Excel, PowerPoint)
• Excellent written and verbal English communication skills
• Strong organizational and problem-solving abilities