Study állás innen: Budapest

2025. 11. 25. | 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

2025. 11. 13. | Teljes munkaidõ | Budapest | 4flowWith your personality, skills, knowledge, and experience You have at least 2 years of practical experience in HR, particularly in people operations You have successfully completed your studies in business administration or a related field of study with a focus on human resources Your communication skills

2025. 11. 13. | Teljes munkaidõ | Budapest | Celanese CorporationDriven Decision making Experience in feasibility study, business case and financial efficiency plans Experience in the following technologies Application packaging, AutoPilot

2025. 11. 13. | Teljes munkaidõ | Budapest | Precision Medicine GroupWill have full service oversight for clinical projects across global/regional (ph I-IV) trials, within Oncology (or Rare Diseases or CNS). Accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality. Involved in all study stages

2025. 11. 13. | Teljes munkaidõ | Budapest | Precision Medicine GroupKnowledge and analysis of the competitive environment and analysis of the study design and rationale. The Director, Operational Strategy will support the business development team by representing Precision operations at pre-award meetings. In addition, this team member will lead specific projects

2025. 11. 13. | 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

2025. 11. 13. | Teljes munkaidõ | Budapest | IQVIAFor SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses. Main Responsibilities and Accountabilities Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited