Clinical Research Associate (CRA)

Roles & Responsibilities

• Conduct onsite monitoring visits in compliance with ICH-GCP guidelines
• Ensure subject safety, data integrity, and protocol adherence
• Review and verify source documents, CRFs, and eCRFs
• Perform site initiation, routine monitoring, and close-out visits
• Identify, document, and report protocol deviations
• Coordinate with investigators, site staff, and internal study teams
• Support regulatory documentation and audit/inspection readiness
• Ensure timely resolution of data queries and follow-up actions

Qualification

• B.Pharm / M.Pharm
• OR Diploma in Clinical Research

Experience

• 1–2 years of onsite clinical trial monitoring experience preferred
• Exposure to site monitoring activities in clinical trials

Skills

• Strong understanding of ICH-GCP, GVP, and clinical trial processes
• Excellent documentation and communication skills
• Ability to coordinate effectively with sites and cross-functional teams
• Willingness to travel for site monitoring visits
• Detail-oriented with strong compliance mindset

About the Organisation

Innovate Research Pvt. Ltd. is a rapidly growing global Clinical Research Organization with operations across India, USA, UAE, UK, and Hungary. Known for its innovation-driven and quality-focused approach, Innovate Research delivers end-to-end clinical research services while maintaining the highest standards of regulatory compliance and patient safety. The organization offers professionals strong exposure to international clinical trials and long-term career growth in the clinical research domain.