Study állás innen: Budapesti Kerület

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 | 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. 19. | Teljes munkaidõ | Budapest | Bosch GroupRelevant RF standards, specifications, protocols and regulations Qualifications - Successfully completed a degree in Electrical Engineering with a specialization in Radio Frequency Engineering or a comparable field of study. - Experience in the development of RF circuits, especially antennas. - Relevant

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

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

2026. 03. 17. | Teljes munkaidõ | Budapest | PSI CROProgramming of patient profiles - Participate and support the development of Study Data Tabulation Model (SDTM) (, annotated CRF, reviewer’s guide) and programming of data transformation from raw data sources into CDISC-complaint deliverable - Validation of clinical trial data according to SDTM

2026. 03. 17. | Teljes munkaidõ | Budapest | PSISubmissions and notifications Coordinates preparation for and follow-up on site, TMF and systems audits and inspections Supports the organization of internal team meetings including preparation of agendas and minutes, and also of Investigator’s Meetings Maintains study-specific and corporate tracking systems