2024. 05. 29. | Teljes munkaidõ | Budapest | haysCTIS Specialist/Regulatory Managers for our CRO Partner. Your responsibilities - Take active part in the start-up activities of Clinical trials - Responsible for coordination of the Regulatory Intelligence procedures and regulatory training in those countries which are allocated to him/her
Nézze később2024. 05. 23. | Teljes munkaidõ | Budapest | haysAssurance in contracts, supplier and subcontractor quality assurance assessmentssupport for process improvement, ensuring compliance with applicable Hungarian laws, GMP, and GMP expectations documented by the local CRO in the country conducting clinical trials - responsibilities include compliance
Nézze később2024. 05. 23. | Teljes munkaidõ | Budapest | haysWith study protocols - Develop and implement a relevant clinical trial data management plan - Work with scientists and relevant personnel to develop data-related SOPs that allow for centralized and remote data monitoring, tracking, and verification of all aspects of clinical trials. - Import existing data
Nézze később2023. 09. 18. | Teljes munkaidõ | Budapest | haysWhat you need to succeed - Bachelor degree in life sciences - 8 years experience in the pharmaceutical industry in quality assurance - Leadership experience or project management - Experience with clinical trials is an advatage - Fluent English (spoken and written) - Driver’s licance - Ability
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Napi új bejegyzéseket kaphat e-mailben a Clinical Trial Assistant Budapesti Kerület.