Study állás innen: Magyarország

2026. 01. 30. | Teljes munkaidõ | Budapest | EYSuitable candidates are open-minded, willing to learn and self-study but also pro-actively contribute to the team and its development. If you have the confidence to

2026. 01. 30. | Teljes munkaidõ | Budapest | AbbViestudy of the publications, literature, guidelines. - Develop and maintain in-depth knowledge for assigned product(s)/ TAs through attendance/ participation at key internal meetings/ training sessions, relevant congresses, and seminars and by regular self-study of the publications, literature, guidelines

2026. 01. 30. | Teljes munkaidõ | Budapesti | ClarioConduct needs analyses, develop high‑level and detailed designs, and create training content from concept through final production and rollout. Partner with internal teams and clients to gather training requirements and ensure content aligns with study, product, and protocol objectives. Produce raw

2026. 01. 30. | Teljes munkaidõ | ICONWhat you will be doing - Building and maintaining strong relationships with key stakeholders at clinical trial sites, including principal investigators, site coordinators, and research staff. - Providing support and guidance to site staff on study protocols, procedures, and regulatory requirements

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 | 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

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 | 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