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23.07.2024
Local Trial Manager
Centurion
... Manager (SM) and Central Trial Manager (CTM)/Global Trial Manager to ensure overall study delivery at the country level. Deliverables: Services rendered will adhere to applicable SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc. Complies with ...
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IQVIA Argentina
03.08.2024
Local Trial Manager
Centurion
... Manager (SM) and Central Trial Manager (CTM)/Global Trial Manager to ensure overall study delivery at the country level.Deliverables:Services rendered will adhere to applicable SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc.Complies with relevant ...
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IQVIA Argentina
27.07.2024
Clinical Trial Assistant
Centurion
... managers, and clients. • Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training. • Knowledge of applicable protocol requirements as provided in company ...
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IQVIA Argentina
23.07.2024
Centralized Monitor, Dutch Speaking
Centurion
... IQVIA Centralized Monitoring Department. A CM provides remote project support and assistance across multiple projects, sites and teams and reviews the structured clinical data output with access to medical charts. What are the responsibilities of a CM? As a CM, you will: Perform centralized ...
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IQVIA Argentina
24.07.2024
Centralized Monitor, Dutch Speaking
Centurion
... IQVIA Centralized Monitoring Department. A CM provides remote project support and assistance across multiple projects, sites and teams and reviews the structured clinical data output with access to medical charts.What are the responsibilities of a CM? As a CM, you will: Perform centralized ...
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IQVIA Argentina
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