PRIMARY PURPOSE:The Sr. Clinical Research Associate (SrCRA) is responsible for monitoring clinical study sites to ensure compliance with clinical trial protocol, to check clinical …
POSITION RESPONSIBILITIES :The Medical Monitor will perform the following activities:- Design develop prepare and initiate clinical study protocols and required documentation in co…
POSITION RESPONSIBILITIES : The Project Manager Independently or in consultation with the Sponsor/CRO will :- Locate and select clinical investigators appropriate to the thera…