2024. 06. 14. | Teljes munkaidõ | Budapest | SanofiReady to challenge the status quo to ensure development and impact of Sanofi's AI solutions for developing the drugs and improving the clinical trials that will benefit the patients of tomorrow. The ideal candidate will have a keen eye for improvement opportunities and a demonstrated ability to deliver
Nézze később2024. 06. 14. | Teljes munkaidõ | Budapest | MOL MagyarországApplications. Determine material requirements or specifications for targeted applications. Communicate material requirements and desired timing to R&D at project initiationSchedules molding trials for material evaluation in actual parts, attending as schedule permitsPresents a formalized data package
Nézze később2024. 06. 14. | Teljes munkaidõ | Budapest | ClarioThe Full Stack Developer R&D will provide software design, development, and application support for Clario products whilst adhering to departmental io is a 50+ year old company that delivers industry leading clinical trial endpoint technology solutions. The future of clinical trials
Nézze később2024. 06. 14. | Teljes munkaidõ | Budapest | Randstad Hungarytrials and commissioning Developing technical solutions, obtaining necessary information Harmonizing technical solutions within the project team Organization of consultations between specialty areas (within and outside of the project, company) Conducting, documenting technical meetings, verifying
Nézze később2024. 06. 14. | Teljes munkaidõ | Budapest | ProclinicalProclinical is collaborating with a organisation to find a dedicated Data Manager. In this role, you will be instrumental in developing and maintaining cloud-based data systems for clinical trial management. Your work will ensure the efficiency and compliance of clinical trials across multiple
Nézze később2024. 06. 14. | Teljes munkaidõ | Budapest | ParexelLead the Parexel and client teams by combining your deep clinical research experience with insight into client pressures in order to develop the right solution for the will provide overall cross-functional leadership of our clinical trials and studies as well as the project teams to achieve
Nézze később2024. 06. 14. | Teljes munkaidõ | Budapest | IQVIA will advise and support the site by resolving any issues or questions that they may have when designing and testing trials, and during the conduct, and collection of data in their clinical may be required to assist with the specification of new features and functionality. The Solutions
Nézze később2024. 06. 14. | Teljes munkaidõ | Budapest | ParexelLithuania, Czechia, Serbia and the Senior Regulatory Affairs Associate you will come with a few years of Regulatory Affairs experience gained in the industry. You will bring experience in Clinical Trial Applications (CTA) from various European locations. You will have a chance to work
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Napi új bejegyzéseket kaphat e-mailben a Clinical Trial Assistant Budapesti Kerület.