Study állás innen: Budapesti Megye

2026. 04. 30. | 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. 04. 30. | Teljes munkaidõ | Budapest | IQVIAColleagues and CRO Partners to review SDTM • In collaboration with Study Data Leads ensure the planning for data receipt and its oversight throughout the duration of assigned clinical trials • Program reports and contribute to the standardization of process and reports used for data review and analysis

2026. 04. 30. | Teljes munkaidõ | Budapesti | ClarioManagement deliverables for assigned studies, ensuring timelines and quality standards are met. Support study setup activities, including eCRF/TF design, database structure, and specifications, obtaining and providing necessary approvals. Understand study implementation and data collection requirements

2026. 04. 29. | Teljes munkaidõ | Budapest | ICONOf a study - Subject matter expertise in the designated therapeutic area - Prior monitoring experience is preferred - Willingness to travel as required (approximately 25%) What ICON can offer you Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture

2026. 04. 28. | Teljes munkaidõ | Budapest | IQVIALead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence and contribute to clinical

2026. 04. 28. | Teljes munkaidõ | Budapest | IQVIALicensing processes, and managed services models. Acts as a subject matter expert for COA/eCOA licensing activities, including license identification, permissions, fee negotiation coordination, contract execution support, and ongoing study support. Identifies opportunities for additional COA, eCOA

2026. 04. 27. | Teljes munkaidõ | Budapest | ICONThe Role As a key member of the clinical unit team, you will support the delivery of clinical trials by ensuring the safety, wellbeing, and accurate monitoring of study participants in both inpatient and outpatient/ambulatory settings, including screening visits. You will work collaboratively

2026. 04. 27. | 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