Study állás innen: Budapesti Kerület

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 | PSI CROJob 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. 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. 24. | Teljes munkaidõ | Budapest | IQVIATo lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations. In addition

2026. 03. 24. | Teljes munkaidõ | Budapest | PurolabsBriefs, and work with editors and creators to produce ads that convert at scale. This is a performance role. Data guides everything. You'll live inside our ad accounts, study what's working, and use those insights to develop the next round of winning creatives. Creative instinct matters, but the numbers

2026. 03. 23. | Teljes munkaidõ | Budapest | ICONTo launch your career in clinical programming with an organisation that invests in your development and values your contribution? At ICON, we’re looking for a motivated Study Lead Programmer to join our diverse, collaborative, and forward‑thinking team. In this role, you’ll support the development

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 | 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