As the Head of Clinical Trial Services Unit, I oversee the comprehensive management of clinical trials, ensuring seamless execution across all phases of project management, packaging, supply chain, and logistics. My role encompasses the end-to-end coordination of sourcing, production planning, Instruments requirement planning at sites to conduct Clinical Trial, regulatory compliance, and quality management for both investigational products and ancillary supplies.

Clinical Drug Packaging and IP supply management

Technical Person for Manufacturing and Packing of Clinical Drug. Clinical Drug Packing and Devlopment of clinical drug packaging

Packaging Executive

Handling daily Manpoer and Packaging Line. Control online Rejection.

• Responsible for handling multiple projects of clients.• Responsible for handling revenue for various clients

Protocol preparation, Case Record Form (CRF) preparation, reviewed Clinical Study Report, Labels for Investigational Product (IP), pre-screening, screening, IP dispensing, sample collection, sample separation, Informed Consent Form (ICF) presentation, reviewed Trial Master File of BA/BE study, Quality Assurance responsibilities.