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06.07.2024
Clinical Research Associate
Centurion
... and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring visits (selection, initiation, monitoring and ...
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IQVIA Argentina
16.08.2024
Associate Medical Safety Director
Centurion
... consultant for any medical support for pharmacovigilance operations.Associate Medical Safety DirectorRole responsibilities:You will be performing medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, ...
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IQVIA Argentina
10.08.2024
Senior Clinical Research Associate
Centurion
... and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and ...
More »
IQVIA Argentina
10.08.2024
Clinical Research Associate
Centurion
... and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and ...
More »
IQVIA Argentina
16.08.2024
Associate Medical Safety Director
Centurion
... consultant for any medical support for pharmacovigilance operations. Associate Medical Safety Director Role responsibilities: You will be performing medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative ...
More »
IQVIA Argentina
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