• Monitor clinical trial sites for protocol compliance
• Perform site initiation, monitoring and close-out visits
• Ensure data quality and regulatory compliance
• Coordinate with investigators and CRO teams
• Maintain trial documentation and reports
B.Pharm / M.Pharm / Pharm.D / MSc / BSc (Life Sciences)
0 – 3 years
• GCP & ICH guidelines
• Clinical monitoring
• Documentation & reporting
• Site coordination
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