Study állás innen: Magyarország

2026. 02. 11. | Teljes munkaidõ | Budapest | PSI CROstudy progress - Participate in feasibility research - Support regulatory team in preparing documents for study submissions - Prepare and participate on audits and inspections Qualifications The successful candidate must possess the following qualifications - Bachelor's degree or higher in Life

2026. 02. 07. | Teljes munkaidõ | Budapest | Thermo Fisher ScientificREQUIREMENTS • Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in customer service, preferably in a scientific, technical, or shared services environment • Preferred Fields of Study Business, Science, Biology, Biotechnology, or related field • Additional

2026. 02. 05. | Teljes munkaidõ | Budapest | ClarioMatter expertise within client facing meetings as required Create and maintain specifications for study-specific implementations of Clario products and services Ensure consistency between trial data capture, data delivery and database structures Collaborate with Clinical Systems Translation & Licensing

2026. 02. 04. | 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. 29. | Teljes munkaidõ | Budapest | IQVIARisk evaluation of drugs in clinical trial and post marketing set up, preparation, and/or contribution to responses to questions from health authorities, reviewing and contributing to periodic aggregate reports, contributing to safety review of study protocols, investigators brochure and other

2026. 01. 29. | Teljes munkaidõ | Parexel& Responsibilities Develop submission strategies and plans for post-approval CMC activities such as variations, renewals, market expansions, and annual reports. Assess change controls and provide regulatory assessments of quality changes in production and quality control. Review study reports from the quality

2026. 01. 29. | Teljes munkaidõ | Szeged | StaphytTasks Set up and monitor tests according to the principles of Good Experimental Practice (GEP), GLP and SEEDS in compliance with protocols/study plans, Standard Operating Procedures, standards and decrees in force in your country. - Site location You determine the test site, according to the specific

2026. 01. 29. | Teljes munkaidõ | Budapest | Parexel& Responsibilities Develop submission strategies and plans for post-approval CMC activities such as variations, renewals, market expansions, and annual reports. Assess change controls and provide regulatory assessments of quality changes in production and quality control. Review study reports from the quality