2025. 07. 06. | Teljes munkaidõ | Budapest | IQVIAWith local medical devices submission experience. Job Profile Summary Prepares, performs and follows-up on submissions to National Competent Authorities (NCAs), Ethical Committees (ECs), Institutional Review Boards (IRB) and other reviewing bodies according to the relevant legislation and guidelines
Nézze később2025. 07. 06. | 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
Nézze később2025. 07. 05. | 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
Nézze később2025. 07. 05. | 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
Nézze később2025. 07. 05. | Teljes munkaidõ | Budapest | IQVIARequirement. Qualifications • Bachelor's degree, scientific discipline or health care preferred • 1-3 years of on-site monitoring experience •
Nézze később2025. 07. 05. | Teljes munkaidõ | Budapest | IQVIACompletion of required training. Qualifications • Bachelor's degree in scientific discipline or health care preferred. • Minimum 6 months of relevant CTA experience. • Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint. • Written and verbal communication skills including
Nézze később2025. 07. 05. | 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
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