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Vacancy description

CRA` in Thana, भारत

IQVIA

  • On-siteWork from the office

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

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