Study start-up: Site feasibility assessment, Site evaluation/selection, Site / Investigator financial & study contract execution, Prepare EC submission packages.
- Site management & clinical study monitoring: Site initiation & liaisoning, Site staff training / re-training, Oversee sites on patient recruitment, Patient retention etc., Site recruitment issue/trouble-shooting, Study monitoring, Source data verification/ensure data quality, Support site audits, Site close out
- Management of clinical trial supplies
- Vendor management
- Project management : Tracking timelines & budget, Site & vendor invoice payments, Coordinate with cross functional teams
Preferred candidate profile: Qualification - M. Pharm/ Pharm D