Clinical Trial Assistant állás innen: Magyarország

2026. 04. 30. | Teljes munkaidõ | Budapest | IQVIAColleagues and CRO Partners to review SDTM • In collaboration with Study Data Leads ensure the planning for data receipt and its oversight throughout the duration of assigned clinical trials • Program reports and contribute to the standardization of process and reports used for data review and analysis

2026. 04. 30. | Teljes munkaidõ | Budapest | IQVIAExpertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers. Senior Clinical Project Managers, IQVIA Biotech are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market

2026. 04. 30. | Teljes munkaidõ | Budapest | DKV MobilityCustomer relationships. Conduct regular customer check-ins to ensure satisfaction and uncover additional sales potential. Sales Activities Deliver persuasive sales presentations, product demonstrations, and trials to potential customers. Provide clear and comprehensive information about DKV products

2026. 04. 30. | Teljes munkaidõ | Budapesti | ClarioBenefits (security, flexibility, support and well-being) Engaging employee programs Remote working and home office allowance OTP Szép Card What you'll be doing Review and evaluate clinical data generated from the imaging portion of sponsor clinical trials across various therapeutic areas. Perform all data

2026. 04. 29. | Teljes munkaidõ | Budapest | ICONOutcomes. Key responsibilities include - Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards. - Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures. - Build and manage strong relationships

2026. 04. 28. | Teljes munkaidõ | Budapest | IQVIALead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence and contribute to clinical

2026. 04. 28. | Teljes munkaidõ | Budapest | IQVIASupport for Phase II-III clinical trials • Independently lead SAP authoring and review • Support integration activities across studies and programs • Act as a proactive statistical partner to Clinical, Programming, and Regulatory teams • Ensure delivery of high‑quality, compliant statistical outputs

2026. 04. 28. | Teljes munkaidõ | Budapest | IQVIAInitiatives, drive operational excellence, and ensure compliant, high-quality outcomes that directly support the success of clinical trials. The role also offers the opportunity to mentor and develop a high-performing delivery team, influence process and product improvements, and contribute to commercial