2026. 04. 28. | Teljes munkaidõ | Budapest | IQVIAWithin a pharmaceutical or CRO setting. Technical Expertise Advanced proficiency in SAS - R for data analysis and statistical programming. Experience with Bayesian methods, predictive modeling, and simulation techniques. Proven track record in strategic study design, including adaptive designs, sample
Nézze később2026. 04. 28. | Teljes munkaidõ | Budapest | PwCOldalról zero trust kezdeményezések szakértői támogatása, megoldások tesztelése, egyeztetése, mint pl CNAPP, XDR, remote access, SASE, stb. Incidens Reagálás és KezelésKiberbiztonsági incidensekre való felkészültségvizsgálata (incident response readiness) vezetése és támogatása, szakértői elemzés
Nézze később2026. 04. 23. | Teljes munkaidõ | Szombathely | AptivTo defined standards, and proper process execution and adherence. Responsibilities and duties Focus area PTP (Supplier MD), DTS (Material MD), OTC (Customer MD) - depending on business needs; Responsible for creating, changing, maintaining, and managing Master Data, PO, SA, and Information in relevant
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. 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 | 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. 26. | Teljes munkaidõ | Budapest | IQVIAParticularly for amendments Good understanding of the Research and Development process (Chemistry, Manufacturing & Controls, Preclinical and Clinical), laws and related guidelines, as appropriate; Strong software and computer skills, including Microsoft Office, CTMS, SA WF, SAFE, Wingspan, as applicable
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