Qualification: M.Pharm

Job Description (CRA)

·  Study start-up : Site identification, evaluation, selection, EC submission dossier preparation, Site contract / CTA
·  Site management for clinical trial : Site initiation & liaisoning, Site staff training, re-training, Oversee sites on patient recruitment, patient retention etc., Site recruitment issue/trouble-shooting, Study monitoring, 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
·  To coordinate with cross functional teams

Interested candidates may share their CVs on vilshashah@torrentpharma.com