Study állás innen: Budapesti Megye

2026. 03. 23. | Teljes munkaidõ | Budapest | Parexel& Responsibilities Develop submission strategies and plans for post-approval CMC activities such as variations, renewals, market expansions, and annual reports. Assess change controls and provide regulatory assessments of quality changes in production and quality control. Review study reports from the quality

2026. 03. 23. | Teljes munkaidõ | Budapest | ICONStandards. You will work closely with Clinical Research Associates (CRAs), site staff, and cross-functional teams to help drive study start-up, maintenance, and close-out activities. What You Will Be Doing - Supporting site activation activities, including the collection, review, and tracking of essential

2026. 03. 23. | Teljes munkaidõ | Budapest | IQVIACommunicate with sponsors and project teams to implement and monitor impact of the recruitment/retention tactical plan; make additional operational and tactical recommendations as needed based on study performance. Collaborate with internal teams and external providers to deliver all appropriate tactics

2026. 03. 23. | Teljes munkaidõ | Budapest | IQVIAWill be working with the client directly to manage deliveries. The CMA contributes to the execution of the Centralized Monitoring process by performing the setup, programming and refresh(es) of the Centralized Monitoring platform, according to the study-specific Centralized Monitoring Plan (CMP). Main

2026. 03. 22. | Teljes munkaidõ | Budapest | IQVIAPerforms review of the Clinical Study Report (CSR) and patient narratives. Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested. Available 24/7 to respond urgent protocol -related questions from investigative sites, in accordance with local labor laws. May require

2026. 03. 21. | 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

2026. 03. 19. | Teljes munkaidõ | Budapesti | ClarioAnd communicate the Data Management Plan (DMP) in collaboration with Sponsors and internal Clinical Data Management teams Determine and document standard and study‑specific edit checks and data processing guidelines to ensure clean, high‑quality data Collaborate with internal teams on study setup requirements

2026. 03. 19. | Teljes munkaidõ | Budapest | ClarioAnd communicate the Data Management Plan (DMP) in collaboration with Sponsors and internal Clinical Data Management teams Determine and document standard and study‑specific edit checks and data processing guidelines to ensure clean, high‑quality data Collaborate with internal teams on study setup requirements