2026. 04. 03. | Teljes munkaidõ | Budapest | IQVIAFeedback in compliance with IQVIA SOP, ICH/ GCP guidelines, protocol requirements and regulatory compliance. Review of the Study Central Monitoring Plan Essential Functions Provide support to CMS leads on clinical deliverables on assigned projects as per the protocol, SOPs, respective regulation/guidelines
Nézze később2026. 04. 02. | Teljes munkaidõ | Budapest | MOL MagyarországFeasibility study preparation, business requirements gathering, dependency graph creations (related to existing and planned services/products) - Provides support in the
Nézze később2026. 04. 01. | Teljes munkaidõ | Budapest | IQVIAJob Overview The role includes responsibilities as an internal financial operational liaison for the Cronos organization, providing end‑to‑end financial oversight across study delivery, internal operations, and strategic planning. This role partners closely with Cronos leadership, Sales Operations
Nézze később2026. 03. 31. | Teljes munkaidõ | Budapest | DeloitteDescription & Requirements Who we are looking for Are you studying in the field of economics? Perhaps you’re in your final/practical semester or just stepping into your career with a diploma in hand (we are primarily looking for students of Finance and Accounting or Business and Management). You
Nézze később2026. 03. 31. | Teljes munkaidõ | Budapest | ParexelStrategy. Contributes from the labeling perspective/labeling environment to Clinical Study designs, protocols, Investigator Brochures and Briefing Books. For the dCCDS/CCDS, leads the interactions with relevant Subject Matter Experts (SMEs) and stakeholders, such as Global Clinical Safety
Nézze később2026. 03. 30. | Teljes munkaidõ | Budapest | Thermo Fisher ScientificBiotech manufacturing or related regulated industry • Preferred Fields of Study Engineering (Chemical, Mechanical, Electrical, Automation, or related field)
Nézze később2026. 03. 28. | Teljes munkaidõ | Budapest | EYSuitable candidates are open-minded, willing to learn and self-study but also pro-actively contribute to the team and its development. If you have the confidence to
Nézze később2026. 03. 26. | Teljes munkaidõ | Budapest | IQVIATo questions from health authorities, reviewing and contributing to periodic aggregate reports, contributing to safety review of study protocols, investigators brochure and other reference safety information, and serving as an internal consultant for any medical support for pharmacovigilance operations
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