Regulator állás innen: Magyarország

2026. 04. 27. | Teljes munkaidõ | Budapest | Citibank Europe plc HungaryTo anticipate, withstand, recover, and adapt to disruptive events. Manage oversight of Third-Party Risk, including risk assessment, contract execution, and exit strategies for external and internal service providers, ensuring alignment with enterprise risk appetite and regulatory standards. Oversee risk

2026. 04. 27. | Teljes munkaidõ | Budapest | IQVIARelevant sponsor or clinical research organization clinical site contracting experience Good negotiating and communication skills with ability to challenge. Strong legal, financial and/or technical writing skills. Strong understanding of regulated clinical trial environment and knowledge of drug

2026. 04. 27. | Teljes munkaidõ | Budapest | EYThe opportunity EY Forensic & Integrity Services helps organizations protect and restore their financial and enterprise reputation. We support companies and legal counsel in investigations, dispute resolution, and regulatory challenges. By putting integrity at the core of compliance programs, we

2026. 04. 27. | Teljes munkaidõ | Budapest | TechBiz Global GmbHFit for you. Key Responsibilities - Ensure compliance with local and international legal and regulatory requirements - Provide legal advice and support to internal teams on business operations - Review, draft, and negotiate contracts and legal documents - Monitor and interpret regulatory changes

2026. 04. 26. | Teljes munkaidõ | Budapest | IQVIAPractice. Remain up to date in all GxP and regulatory requirements applicable to the role. Leads client and vendor related meetings where necessary to discuss Clinical Supply Chain topics or status updates. Provides administration support to the Clinical Trial Supplies team where required Manages

2026. 04. 26. | Teljes munkaidõ | Tatabánya | ColoplastAnd a strong methodological approach Knowledge of applicable regulatory and quality standards within the Medical Device industry Willingness to travel

2026. 04. 26. | Teljes munkaidõ | Budapest | IQVIAJob Description Prepares and/or reviews regulatory documents to support clinical trial submissions. With guidance from senior staff, provides regulatory support for more complex projects. Acts as a Clinical Trial Regulatory Manager (CTRM) on straightforward projects independently and complex

2026. 04. 26. | Teljes munkaidõ | Budapest | PCZ Medtronic Czechia SROPortfolio, ensuring alignment with business objectives, market needs, and regulatory requirements Product Lifecycle Management Oversee the entire lifecycle of capital products, from market analysis and product development to commercialization and end-of-life management Customer & Market Insights Analyze