Posted:2 months ago|
Platform:
Work from Office
Full Time
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 & liaison Ing, 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 M.Sc / M. Pharma with relevant CRA experience of 2-7 Years Interested Candidates can share their CVs on vilshashah@torrentpharma.com
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Pharmaceutical Manufacturing
10001 Employees
57 Jobs
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