Clinical Research Associate II

Role & Responsibilities

• Perform onsite monitoring visits in compliance with ICH-GCP and SOPs
• Conduct interim monitoring visits as per study protocol and timelines
• Ensure subject safety, data integrity, and protocol compliance
• Review source documents, CRFs, and essential trial documents
• Identify, document, and resolve site issues and deviations
• Liaise with investigators, site staff, and study teams
• Ensure timely follow-up and closure of monitoring findings
• Maintain accurate monitoring reports and documentation

Qualification

• B.Pharm / M.Pharm / Pharm.D
• BHMS / BAMS / BDS

Experience

• Minimum 2+ years of onsite clinical monitoring experience
• Completion of at least 90+ onsite interim monitoring visits (mandatory)

Skills

• Strong knowledge of ICH-GCP and clinical trial regulations
• Excellent documentation and report writing skills
• Good communication and stakeholder management skills
• Strong attention to detail and compliance mindset
• Ability to work independently in a field-based role

About Company

• IQVIA is a global leader in clinical research, healthcare intelligence, and data-driven innovation , Offers a diverse, inclusive, and growth-oriented work culture , Committed to improving patient outcomes through science and technology