Study állás innen: Magyarország

2026. 01. 23. | Teljes munkaidõ | Budapest | Thermo Fisher ScientificBiotech manufacturing or related regulated industry • Preferred Fields of Study Engineering (Chemical, Mechanical, Electrical, Automation, or related field)

2026. 01. 23. | Teljes munkaidõ | Budapest | IQVIAUsed to access, extract, transform, review, analyze and submit clinical data for all requested analyses. Main Responsibilities and Accountabilities Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM

2026. 01. 23. | Teljes munkaidõ | Budapest | IQVIAJob Overview Manage the execution of the assigned clinical study (ies) from initiation through to closeout. Ensure that clinical study management and project deliverables are on time and is in accordance with standard operating procedures (SOPs), policies and practices. To provide project related

2026. 01. 23. | Teljes munkaidõ | Budapest | IQVIAJob Overview Clinical Research Associate performs monitoring and site management work to ensure that sites are conducting the studies and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site

2026. 01. 23. | Teljes munkaidõ | Budapest | IQVIAClinical Trial Educators (CTEs) collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance. They lead

2026. 01. 22. | Teljes munkaidõ | Gyöngyös | Procter & GambleWith the business requirements. Define and evaluate technical options for achieving business objectives. Study technical feasibility and capital cost of proposed changes. Prepare a design basis for the project, based on engineering studies, computer modeling and simulation, economic evaluations, and consultations

2026. 01. 22. | 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. 01. 21. | Teljes munkaidõ | Budapest | ExcelyaExpertise required for the successful completion of Excelya’s projects. Your Mission - Produce high‑quality scientific content in clinical medical writing (including clinical protocols, informed consent forms, clinical study reports, lay summaries), regulatory medical writing (CTDs 2.5-2.7) and medical