Study állás innen: Magyarország

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. 25. | Teljes munkaidõ | Budapest | ParexelTrials, acts as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data. What You'll Do At Parexel • Create SAS programs to generate

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

2026. 03. 25. | Teljes munkaidõ | Budapest | PSI CROstudy sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines - Advise clients, project teams, sites, regulatory agencies and third-party vendors on medical matters - Collaborate with internal departments in the preparation of clinical

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. 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

2026. 03. 11. | Teljes munkaidõ | Budapest | Thermo Fisher ScientificAnd transformational changes that enhance operational efficiency and customer success. REQUIREMENTS • Advanced degree plus 6 years of experience, or Bachelor's degree plus 8 years of experience, managing complex, cross-functional initiatives • Preferred Fields of Study engineering, business, science, or related