Job Overview
Under Supervision, Provide a wide range of medical surveillance support (including monitoring of clinical laboratory data for subjects in clinical
studies and  composing medical narratives and interfacing with investigator sites.)

Essential Functions
• Under Supervision   evaluating  and analyzing  laboratory results on a daily basis,from sponsor designated central laboratory and/or data management system
• Under Supervision conduct  the monitoring of Laboratory safety parameters for each patient at every site throughout clinical drug trial
• Under Supervision conducts preliminary review of laboratory results relative to established protocol-specific reference range guidelines
• Follow established procedure for comparing current results with prior laboratory values to identify trends or potentially clinically significant increases/decreases, Under supervision, contacts the investigator site for pertinent additional clinical assessment, and consults with Sponsor/IQVIA physicians for medical evalution

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com