Study állás innen: Magyarország

2026. 03. 26. | Teljes munkaidõ | ParexelStrategy. Contributes from the labeling perspective/labeling environment to Clinical Study designs, protocols, Investigator Brochures and Briefing Books. For the dCCDS/CCDS, leads the interactions with relevant Subject Matter Experts (SMEs) and stakeholders, such as Global Clinical Safety

2026. 03. 26. | Teljes munkaidõ | Budapest | IQVIATo questions from health authorities, reviewing and contributing to periodic aggregate reports, contributing to safety review of study protocols, investigators brochure and other reference safety information, and serving as an internal consultant for any medical support for pharmacovigilance operations

2026. 03. 25. | Teljes munkaidõ | Szeged | StaphytExperimental 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 conditions. You set up the test site with appropriate equipment. Treatments

2026. 03. 25. | Teljes munkaidõ | Szeged | StaphytExperimental 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 conditions. You set up the test site with appropriate equipment. Treatments

2026. 03. 25. | Teljes munkaidõ | Budapest | PSI CROJob Description PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being. Responsibilities - Serve as medical point of contact for internal project team, study sites and study sponsor

2026. 03. 25. | Teljes munkaidõ | Budapest | SanofiThe global supply of investigational products to study participants worldwide, serving as the primary country contact for all IMP-related matters across your assigned studies. Main responsibilities Study Setup and Implementation Identify and implement efficiency gains in the management of IMP/AxMP/MD

2026. 03. 25. | Teljes munkaidõ | Budapest | ParexelTrials, acts as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data. What You'll Do At Parexel • Create SAS programs to generate

2026. 03. 24. | Teljes munkaidõ | Budapest | IQVIAGlobal Trial Delivery Manager services provide for the global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure global clinical operations deliverables progress according to agreed