Clinical Research Associate, with on site monitoring experienceHungary basedIQVIA Hungary is looking for a talented and motivated team member to join our Sponsor dedicated departme...
Site Manager Study Start UpReal World EvidenceEMEA basedJoin us on our exciting journey!IQVIA Real World Evidence (RWE) teams work with clients to help them collect and use real wo...
IQVIA Safety Operations team play an important part in the design, build and execution of end to end safety solutions for major pharmaceutical companies and their post market produ...
Job OverviewThis position is responsible for providing line management to an assigned data management team. This role is also responsible for delivering strategic solutions and pro...
Associate Site Manager with FrenchReal World EvidenceHybrid. EMEAJoin us on our exciting journey!IQVIA Real World Evidence (RWE) teams work with clients to help them collect and us...
Prepares and or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts...
Country Site ActivationJoin us on our exciting journey!IQVIA's Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure pa...
Prepares and or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a C...
Job OverviewWe are looking to hire a (Sr) Site Activation Coordinator to perform administrative tasks at a country level in accordance with applicable local and or international re...
The Global Finance Automation & Analytics team is tasked with digitalizing the workspace fostering a culture of continuous improvement in our business processes through automation ...
Who are we?We are the creators of ClinSpark , the world's first CDISC ODM certified Phase I eSource and clinical trial automation system. ClinSpark (now known as 'IQVIA Clinical eS...
Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and or international regulations, standard operatin...
DevOps EngineerFlexible location across Europe, home basedAbout the roleYou'll be part of a very tight, highly professional team comprised of domain experts, former clinical resear...
The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territ...
IQVIA. je vodeća kompanija za proučavanje ljudskih podataka fokusirana da pomogne zdravstvenim klijentima da imaju najbolji uvid i još bolja rešenja za pacijente. IQVIA nudi širok...
IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical tri...
Job ResponsibilitiesProvide line and functional management of Data Management technical experts, with a team size of around 15 20 people.Manage and prioritize resource assignments,...
Office based position in Budapest, Hungary.Job OverviewUnder general supervision, provide remote second tier Information Technology (IT) support to end users, to restore service an...