03.06.2024 | Full-time | Oradea | PharmiwebOf site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Manage progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Collaborate
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebOf site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Manage progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Collaborate
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebSenior Clinical Research Associate IQVIA is the Human Data Science Company oriented to drive human health outcomes forward. When you join IQVIA Bucharest as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct
Uita-te mai târziu03.06.2024 | Full-time | PharmiwebOf site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Manage progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution. Collaborate
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 | PharmiwebAnd the corresponding training records are complete and accurate at any time point during all trial phases. Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target. Ensures quality data (accurate, valid
Uita-te mai târziu03.06.2024 | Full-time | Cluj-Napoca | 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 | PharmiwebPartners. Work collaboratively in the pursuit of quality with the primary site monitor, the Study Team and cross-functional departments. Qualifications Bachelors degree in related field, may include life sciences, risk-based discipline; Minimum of 2 years of clinically related or data trend analysis
Uita-te mai târziu03.06.2024 | Full-time | L'OréalCalling all innovators, disruptors, and dreamers! Join L’Oréal, the world's beauty company present in over markets. For over years, we’ve been transforming, fueled by data, tech, innovation, and science. Together, we solve complex challenges at scale, while staying true to our commitments
Uita-te mai târziu03.06.2024 | Full-time | ContinentalMeasurements. Ensure IT security, IT compliance and Enterprise Architecture Management principles;Coordination of the technical teams and experts from SAP System provider, SAP Basis, Infrastructure and SAP Group Sectors;Supports the selection process for the main components;Supports infrastructure
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