2026. 04. 21. | 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
Nézze később2026. 04. 21. | Teljes munkaidõ | Budapest | ICONThe Nordic region (Sweden, Norway, Denmark, and Finland). As a Site Specialist I at ICON, you will be at the heart of study start-up, ensuring essential documentation and site activation activities are delivered efficiently, compliantly, and with a strong sense of partnership. Your work will directly
Nézze később2026. 04. 21. | Teljes munkaidõ | Budapest | Nucs AIMedical community. Working alongside the Medical Director and Associate Director of Medical Programs, you’ll translate clinical insights and study results into compelling scientific narratives, educational programs, and market-facing materials that build trust and drive adoption. You’ll also manage
Nézze később2026. 04. 21. | 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
Nézze később2026. 04. 21. | 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
Nézze később2026. 04. 19. | Teljes munkaidõ | Budapest | Precision Medicine GroupPosition Summary The Senior Clinical Data Manager/Principal Clinical Data Manager is responsible and manages all aspects of the clinical trial data management process from study start up to post database lock for assigned projects. Standard Operating Procedures - Work Instructions (SOPs/WIs
Nézze később2026. 04. 19. | Teljes munkaidõ | Budapest | foodoraIn briefing, negotiation and coordination. - You’ll use both your English and Hungarian daily, and have the chance to strengthen your communication skills in both. Qualifications What we’re looking for - You're currently a university student, ideally studying Business, Marketing, Communication or a related
Nézze később2026. 04. 18. | Teljes munkaidõ | Budapest | SanofiFor Clinical Operations (DICO) team as an Operational Data Steward Leader and you’ll be accountable for the strategy and coordination of the E2E governance of clinical operational data study design characteristics, study stakeholders (study team members, vendors, investigational sites, HCPs…), study
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