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17.09.2024
Centralized Monitor, Dutch Speaking
Centurion
... data analysis? Understands clinical trial conduct, and skill in applying applicable clinical research regulatory requirements and relevant local laws, regulations and guidelines? Able to communicate efficiently and work well across cultures and geographies? Can you speak, read and write Dutch? ...
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IQVIA
18.09.2024
Global Site Activation Manager, South Africa
Centurion
... database and best in class systems to enable the start-up strategy execution. The Site Activation Manager is a fundamental role to deliver our clinical trial portfolio and belongs to a global unit with vast career growth opportunities. Qualifications Bachelor's Degree, Master's Degree, or Ph.D. ...
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IQVIA
18.09.2024
Senior Clinical Research Associate
Centurion
... 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 visits) in accordance with contracted scope of work and Good Clinical Practice. Work with ...
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IQVIA
18.09.2024
Clinical Research Associate 2 - Sponsor Dedicated
Centurion
... 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 visits) in accordance with contracted scope of work and regulatory requirements, i.e., ...
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IQVIA
15.09.2024
Global Site Activation Manager, South Africa
Centurion
... database and best in class systems to enable the start-up strategy execution. The Site Activation Manager is a fundamental role to deliver our clinical trial portfolio and belongs to a global unit with vast career growth opportunities. Qualifications Bachelor's Degree, Master's Degree or Ph.D ...
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IQVIA Argentina
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