Assist with site file maintenance, Investigator Site File organisation, and basic Case Report Form( CRF) completion review for assigned studies
- Support patient recruitment coordination and screening log maintenance under CRA supervision
- Learn segment-specific documentation requirements across Pharma Regulatory, Medical Device, and AYUSH/Nutraceutical studies
- Shadow senior CRAs on site initiation, monitoring, and close-out visits to build toward independent site management
- Support routine data query resolution and follow-up documentation
- Assist with study-level administrative tasks, including courier tracking, supply management, and meeting scheduling
- Maintain accurate records of training completion and site-specific requirements per study protocol