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Clinical Trial Associate Veeda CR

1.0 - 3.0 years

2 - 4 Lacs

ahmedabad

Work from Office

Role & responsibilities EC Submission • To get the documents from Central Drive, print, prepare files accordingly, and dispatch them to the respective sites prior to the Ethics Committee meeting conducted at site. SIV (Site Initiation Visit) Kits Preparation • To co-ordinate with CRD and prepare the SIV kits, study related material (NS Bottle, Syringe & Needle, Instrument- Digital clock, thermo hygrometer, Data logger, Infusion Pump) and dispatch to the site before the Site Initiation Visit. Logistics Activities • To arrange the IMP (Investigational Medicinal Product) shipments at the site, coordinate with the Pharmacist Team & logistics vendor before patients randomize the study. • To arran...

Posted 1 hour ago

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