1. Managing regulatory authority/IRB applications and approvals
2. Coordinates and executes clinical research activities for assigned products and supports the evaluation of new products
3. Provides technical input to study protocols and assigned studies through all phases of the study process
4.Train and manage study sites and conduct/document study per protocol using GCP guidelines and SOPs
5.Preparation of clinical trial budgets and tracking of expenditure
6. Liaison with CRO responsible for trial-related activities