Study állás innen: Magyarország

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. 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 | 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 | 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

2026. 03. 17. | Teljes munkaidõ | Budapest | PSIOf 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 specifications

2026. 03. 17. | Teljes munkaidõ | Budapest | PSISpecialist Communicate and build relationship with clinical sites to identify potential centres for clinical trials. Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement Project Responsibilities Conduct site identification activities

2026. 03. 14. | Teljes munkaidõ | Budapest | Nucs AIPrograms function to support our expanding portfolio of clinical collaborations, validation studies, and regulatory evidence generation. This is a new role designed to own the operational execution of our medical programs-from clinical study coordination and site management to data collection, protocol