Warsaw, Mazowieckie, Poland- Planning, preparing, handling, distributing and submitting regulatory documents to Health Authorities and/or Marketing Companies, globally, in support of clinical trials. - Providing regulatory expertise on clinical trial related submissions to cross functional teams - Monitoring, interpreting and validating current and changing regulatory legislation in relation to clinical trials and shar...
Kyiv City, Ukraine- Maintain the paper and electronic Central Files for Clinical Operation, ensuring efficiency, accuracy and quality.
- Tracking, scanning, filing, entry and return of Case Report Forms to clients for assigned projects, upload and naming of documents in accordance with naming convention to the electronic document management system, EDC User Management activities.
- Maintain basic quality check...