Guide Experience állás innen: Magyarország

2025. 07. 04. | Teljes munkaidõ | Budapest | IQVIADesign, and a culture of continuous improvement. You will help guide the transformation of machine learning research domain expertise in the areas of human data into viable prototypes. Your technical leadership will enable our Machine Learning Engineers to build and train new production-grade algorithms

2025. 07. 03. | Teljes munkaidõ | Budapest | IQVIAMinimum 4 years of experience in post-approval regulatory affairs for the EU market. Fluent in English (C1 or above). Solid understanding of the R&D process (especially CMC), EU regulatory guidelines, and submission procedures. Strong organizational and time management skills. Proficiency in Microsoft

2025. 07. 02. | Teljes munkaidõ | Budapest | IQVIAOf external research and data with IQVIA’s internal data sources. Guide and mentor assigned Project Leader so that they can confidently present the project strategy to the client and the internal stakeholders. Actively support Sales in the preparation and conduct of customer and bid defense meetings e.g

2025. 07. 01. | Teljes munkaidõ | Budapest | IQVIAProtocol, company Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through close-out. Takes ownership for assigned responsibilities. Demonstrated competency to act as a backup or first point of contact in absence of the GCDO

2025. 06. 28. | Teljes munkaidõ | Budapest | IQVIAProtocol, company Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through close-out. Takes ownership for assigned responsibilities. Demonstrated competency to act as a backup or first point of contact in absence of the GCDO

2025. 06. 27. | Teljes munkaidõ | Budapest | IQVIASubject safety, data integrity, escalation of issues and timely and responsive feedback in compliance with IQVIA SOPs, International Conference on Harmonization - Good Clinical Practice (ICH GCP) guidelines, protocol requirements and regulatory compliance. Develop and use of study management plans

2025. 06. 26. | Teljes munkaidõ | Budapest | IQVIADevelopment. The Cardiovascular Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical trials who will be a champion for Cardiovascular across IQVIA. The key remit of the role is drive growth of the IQVIA Cardiovascular portfolio through scientific and clinical

2025. 06. 26. | Teljes munkaidõ | Budapest | IQVIATimelines. With moderate oversight and supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May