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

Solid 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

📌 Clinical Research Associate - monitoring experience required (Thane)
🏢 Iqvia
📍 Thane