Study állás innen: Magyarország

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. 31. | Teljes munkaidõ | Budapest | PSI CROYou will - Coordinate review and negotiation of clinical trial agreements and investigator grants between PSI staff and study sites. - Perform administrative activities (documents collection/distribution, filing clinical trial agreements in the database and maintenance of local documentation

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 | 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 | 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 | 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. 28. | Teljes munkaidõ | Budapest | PSISubmissions and notifications Coordinates preparation for and follow-up on site, TMF and systems audits and inspections Supports the organization of internal team meetings including preparation of agendas and minutes, and also of Investigator’s Meetings Maintains study-specific and corporate tracking systems

2026. 01. 28. | Teljes munkaidõ | Budapest | PSI CROCommittee submissions and notifications - Coordinates preparation for and follow-up on site, TMF and systems audits and inspections - Supports the organization of internal team meetings including preparation of agendas and minutes, and also of Investigator’s Meetings - Maintains study-specific and corporate