2024. 05. 23. | Teljes munkaidõ | Budapest | IQVIAOf requirements and timelinesUse and promote the use of established standards, SOPs, and standard methodologiesExport data and clinical study report materialsProvide training and mentoring to team members and department staffYou can help us bring clinical trial statistical analysis into the next generation. Award
Nézze később2024. 05. 23. | Teljes munkaidõ | Budapest | IQVIAClinical trial justifications with minimum support of senior staffMay strategically plan and perform European centralized submissions and facilitate global submissionsMay provide support on regulatory business development opportunities and complete Data Informed Protocol Assessments (DIPAs)Understands
Nézze később2024. 05. 23. | Teljes munkaidõ | Budapest | IQVIAOr more programs enabling planning, coordination, and timely delivery of complete, high quality and reliable clinical trial data for regulatory approval and market acceptanceLead a Functional Department of Data Management staff. Size of team could vary from 15-40, and may be a first-line or second-line
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