Clinical Operations Executive

*Role & responsibilities :

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

Experience - having worked as CRA

*Willingness to travel 20-25 days in a month