I’m a Doctor of Pharmacy graduate with several years of professional experience in the clinical research and pharmaceutical industry. I have worked with leading organisations like Sanofi, BMS, IQVIA, and AIG Hospitals, supporting global clinical trials and working closely with study teams, investigators, and vendors.

💼 Experience
• 4+ years of experience in clinical trial management, site monitoring, centralized monitoring, and trial documentation (TMF/eTMF)
• Hands-on knowledge of systems like CTMS, EDC, IVRS, and SharePoint
• Strong understanding of ICH-GCP guidelines, regulatory processes, and study start-up to closeout phases
• Supported Phase II and III clinical trials globally
• Certified in Risk-Based Monitoring, Study Management, and Protocol & ICF Preparation

ns can be personalized based on your learning goals—be it understanding TMF, central monitoring, GCP, or study budget tracking.

🌐 Mode of Classes
I offer online classes via Zoom or Google Meet with flexible scheduling on weekdays
and weekends