Study állás innen: Budapest

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. 24. | Teljes munkaidõ | Budapest | IQVIAGlobal Trial Delivery Manager services provide for the global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure global clinical operations deliverables progress according to agreed

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. 24. | Teljes munkaidõ | Budapest | IQVIAAnd countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan. Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate

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

2026. 03. 18. | Teljes munkaidõ | Budapest | IQVIAEffective communication with project team through oral and written correspondence, status reports to ensure alignment with study timelines. Funtions Assists in the review, development and writing of clinical trial documents and manuals, including but not limited to study manuals, laboratory or biomarker

2026. 03. 18. | Teljes munkaidõ | Budapest | TechBiz Global GmbHResponsibilities - Perform statistical programming activities for clinical trials, including early-phase projects, indications, and publications - Lead at least one study team, providing technical and domain expertise - Manage and mentor a small team of 2-4 programmers (if required) - Develop and validate SAS