03.06.2024 | Full-time | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | Full-time | Oradea | PharmiwebEstablished data review guidelines on Fortrea or client data management systems Requirements Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines Excellent understanding of Serious Adverse Event (SAE) reporting Ability to resolve project
Uita-te mai târziu03.06.2024 | Full-time | Craiova | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebEstablished data review guidelines on Fortrea or client data management systems Requirements Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines Excellent understanding of Serious Adverse Event (SAE) reporting Ability to resolve project
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebEstablished data review guidelines on Fortrea or client data management systems Requirements Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines Excellent understanding of Serious Adverse Event (SAE) reporting Ability to resolve project
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebEstablished data review guidelines on Fortrea or client data management systems Requirements Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines Excellent understanding of Serious Adverse Event (SAE) reporting Ability to resolve project
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebEstablished data review guidelines on Fortrea or client data management systems Requirements Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines Excellent understanding of Serious Adverse Event (SAE) reporting Ability to resolve project
Uita-te mai târziu03.06.2024 | Full-time | Oradea | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebFor clinical studies across various phases, ensuring adherence to applicable regulations and principles of ICH-GCP. Responsibilities Travel to sites to carry out site selection, initiation, monitoring and close-outs. Support the development of a subject recruitment plan. Evaluate the quality and integrity
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebInitiation, monitoring and close-out visits Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Managing
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