Study állás innen: Magyarország

2026. 03. 26. | Teljes munkaidõ | Budapest | PSIJob Description PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being. Responsibilities Serve as medical point of contact for internal project team, study sites and study sponsor

2026. 03. 26. | 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. 26. | Teljes munkaidõ | Budapesti | ClarioAre currently seeking an Imaging Research Associate I to join our Medical Imaging business unit in Budapest, Hungary. This role plays a key part in coordinating site and operational activities across the full study lifecycle, from start‑up through close‑out, helping ensure the successful delivery of high

2026. 03. 26. | Teljes munkaidõ | Budapest | IQVIAStep into a role where strategy meets impact. As a Clinical Supply Chain Manager, you will shape and drive the end‑to‑end supply strategy for new clinical trials. Using your ability to translate complex study protocols into smart kit designs and robust supply plans, you’ll ensure that every element

2026. 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

2026. 03. 26. | Teljes munkaidõ | 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. 25. | Teljes munkaidõ | ExcelyaFrom MDD to MDR. - Respond to regulatory authority queries with clear, evidence‑based medical justifications. - Collaborate with cross‑functional teams to support study‑related documentation (protocols, study reports) for medical device projects. - Participate in scientific meetings and stay updated

2026. 03. 25. | Teljes munkaidõ | Budapest | SanofiThe global supply of investigational products to study participants worldwide, serving as the primary country contact for all IMP-related matters across your assigned studies. Main responsibilities Study Setup and Implementation Identify and implement efficiency gains in the management of IMP/AxMP/MD