Study állás innen: Budapesti Megye

2026. 04. 26. | Teljes munkaidõ | Budapest | IQVIAAvailable in accordance with the project requirements. Initiate packaging campaigns with the assigned vendor and provide oversight to ensure on-time delivery Monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems to ensure study inventory is effectively managed

2026. 04. 26. | Teljes munkaidõ | Budapest | IQVIAPerforms review of the Clinical Study Report (CSR) and patient narratives. Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested. Available 24/7 to respond urgent protocol -related questions from investigative sites, in accordance with local labor laws. May require

2026. 04. 24. | Tréning, Teljes munkaidõ | Budapest | FrieslandCampinaWhat we ask Currently following a study in Human Resource Management, Psychology, Business Administration or Training & Development; Excellent communication (spoken and written) in English and Greek language; You have strong knowledge of Excel and other MS Office tools; You are eager to learn

2026. 04. 24. | Teljes munkaidõ | Budapest | ICONMonitoring patient safety and addressing any clinical issues that arise during the course of trials. - Collaborating with biostatisticians and data managers to analyze study data and provide clinical insights. - Engaging with investigators and site staff to facilitate effective trial management

2026. 04. 24. | Teljes munkaidõ | Budapest | ICONThe Nordic region (Sweden, Norway, Denmark, and Finland). As a Site Specialist I at ICON, you will be at the heart of study start-up, ensuring essential documentation and site activation activities are delivered efficiently, compliantly, and with a strong sense of partnership. Your work will directly

2026. 04. 24. | Tréning, Teljes munkaidõ | Budapest | FrieslandCampinaWhat we ask Currently following a study in Human Resource Management, Psychology, Business Administration or Training & Development; Excellent communication (spoken and written) in English, Dutch, Greek language knowledge is an advantage; You have strong knowledge of Excel and other MS Office tools

2026. 04. 24. | Teljes munkaidõ | Budapest | ICONstudy conduct. - Performing data review and resolution of queries to maintain high-quality clinical data. - Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile You will bring relevant clinical trial monitoring experience, along

2026. 04. 23. | Teljes munkaidõ | Budapest | PSI CROTo the area of expertise to site team members involved in patient recruitment - Identify, track, and report patient enrollment progress throughout the study - Analyze the protocol in order to provide the site with the support needed to improve the patient pathway - Provide support to the project teams