03.06.2024 | Full-time | CluePointsAlgorithms to determine the quality of clinical trial data to enable risk planning & operational risk monitoring and have taken the Pharmaceutical industry by storm! As part of our continuous growth, new product introduction and market expansion, we're seeking additional Lead Engineer's to join our dynamic
Uita-te mai târziu03.06.2024 | Full-time | Diebold NixdorfTo ensure our software products’ capabilities to enable retailers for introducing innovative and differentiating consumer and staff journeys. Location Katowice, flexible work will be considered Responsibilities Analyze demands and data provided by retailers, analysts and other market participants
Uita-te mai târziu03.06.2024 | Full-time | Craiova | 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 | 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 | 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 | British American TobaccoIn the digitalization project of Financial Planning and Reporting department. The ideal candidate should be able to design, develop, test and deploy PowerBI dashboards based on predefined business objectives. Experience with data modelling and visualization is critical along with a strong collaborative and solution
Uita-te mai târziu03.06.2024 | Full-time | Craiova | 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 | 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 | 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 | Citibank Europe plc RomaniaImportantly, ICM (CRMS) will coordinate with credit management groups to ensure full alignment on business and regulatory goals, as well as consistency and best practices where covers the following areasCredit Risk Approval ControlsCredit Risk ReportingCRMS Controls and Data QualityCredit
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