03.06.2024 | 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 | PharmiwebIn accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions Collaborating with experts at study sites and with client
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 | 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 | 3Pillar GlobalOf pipelines and re data accuracy, integrity, privacy, security, and compliance through quality control mum QualificationsDemonstrated expertise with a minimum of 5+ years of experience as data engineer or similar role. Advanced SQL skills and experience with relational databases
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 | 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 | GetronicsPrevious work experience as a Security Design & Transition Consultant Experience of integrating Solution with ITSM tools such as ServiceNow Technical knowledge of database and operating system security Hands on experience in security systems, such as firewalls, intrusion detection systems, antivirus
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