Study állás innen: Magyarország

2026. 03. 24. | Teljes munkaidõ | Budapest | IQVIATo lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations. In addition

2026. 04. 11. | Teljes munkaidõ | Budapest | Charles RiverExperience in the field of transporter proteins, drug metabolizing enzymes, cell toxicity, pharmacokinetics Experience in laboratory automation related programming Job Summary Plan and perform drug discovery contract research studies using liquid handling platforms Study related client communication

2026. 04. 11. | Teljes munkaidõ | Budapest | Charles River Laboratories, Inc.Discovery and Development - Experience in the field of transporter proteins, drug metabolizing enzymes, cell toxicity, pharmacokinetics - Experience in laboratory automation related programming Job Summary - Plan and perform drug discovery contract research studies using liquid handling platforms - Study

2026. 04. 11. | Teljes munkaidõ | Budapest | DeloitteTechnology Team we are looking for an ambitious Senior IT Business Analyst! You will definitely make a good impression on us if you have university/college degree in appropriate field of study or relevant work experience but ideally IT with business interests or Economic sciences with IT interests 3 years

2026. 04. 10. | Teljes munkaidõ | Budapest | IQVIAStep into a role where strategy meets impact. As a Clinical Supply Chain Manager, you will shape and drive the end‑to‑end supply strategy for new clinical trials. Using your ability to translate complex study protocols into smart kit designs and robust supply plans, you’ll ensure that every element

2026. 04. 10. | Teljes munkaidõ | Budapest | ICONFor clinical trials, contributing to the successful enrolment of study participants and the delivery of high-quality clinical research. You will work closely with experienced colleagues and cross-functional teams to help implement recruitment strategies, support participant engagement, and ensure recruitment

2026. 04. 09. | Teljes munkaidõ | Budapest | SanofiAs a Trial Master File (TMF) Manager and you’ll be the part of supporting global activities related to the TMF, ensure inspection readiness, provide clinical documents for submissions and participate in continuous improvement initiatives. As part of the study Clinical team you will ensure TMFs are Inspection

2026. 04. 09. | Teljes munkaidõ | Budapest | IQVIAUsed 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 to ADaM