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Yesterday
Senior Clinical Research Associate - West Africa (French speaking)
Bloemfontein
... 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
18.09.2024
Global Site Activation Manager, South Africa
Bloemfontein
... 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
18.09.2024
Centralized Monitor, Dutch Speaking
Bloemfontein
... 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
30.08.2024
Snr Data Team Lead
Bloemfontein
... management services for single/multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet customer ...
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IQVIA LLC
28.07.2024
Associate Client Services Lead (anywhere in Europe)
Bloemfontein
... management projects, and ensures sponsor satisfaction is achieved. Manage and oversee the initiation and study management of protocols including identifying all protocol-related information, timelines, reporting, and initial setup of the proprietary software system used to initiate studies. ...
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IQVIA LLC
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