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16.08.2024
Associate Medical Safety Director
Centurion
... management and benefit-risk evaluation of drugs in clinical trial and post marketing set up, safety aggregate report review, safety review of study protocol, investigators brochure and other reference safety information, clinical study report narrative review, providing medical assessment ...
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IQVIA Argentina
23.07.2024
Centralized Monitor, Dutch Speaking
Centurion
... management and prioritization? Skilled at software and computer use, that enjoys technology applied to data analysis? Understands clinical trial conduct, and skill in applying applicable clinical research regulatory requirements and relevant local laws, regulations and guidelines? Able to ...
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IQVIA Argentina
Yesterday
Senior CEVA Specialist
Centurion
... management and service delivery excellence of projects, as assigned by Clinical Event Validation and Adjudication (CEVA) management, covering single or multiple EAM (Endpoint Adjudication Management) and OGM (Oversight Group Management) projects. Provide leadership and accountability for all ...
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IQVIA Argentina
Yesterday
Senior Clinical Research Associate
Centurion
... 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 close-out ...
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IQVIA Argentina
Yesterday
Global Site Activation Manager, South Africa
Centurion
... IQVIA Global Site Activation team is one of the clear market leaders in Clinical Trial Site Activation, driving best in class employee, site and customer experiences. This position can be anywhere in Europe, remote. Job Overview As a Global Site Activation Manager, you will be our project ...
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IQVIA Argentina
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