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...
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...
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...
Role Overview The Site Enablement Solutions team at IQVIA provides qualified, clinically experienced research staff to clinical trial sites globally to accelerate and optimize the ...
Job OverviewThe medical department consists of a Chief Medical Officer, Medical Directors, medical writers, and safety associates. The Medical Director provides medical and scienti...
Join us on our exciting journey!IQVIA. is The Human Data Science Company , focused on using data and science to help healthcare clients find better solutions for their patients. Fo...
The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territ...
Clinical Data Managers with 4. years of experience of handling third party data, drafting data transfer specification document. Good understanding of protocol and study design to d...
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...
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...
We have great opportunities for those with a background working in Clinical Trials, preferably with a focus on patient recruitment engagement, to join our Site and Patient Networks...
Job OverviewManages a single department or work unit responsible for site activation. Sets goals and objectives for team members for achievement of short term operational or tactic...
Job OverviewAnalyses financial and business performance leveraging key indicators, develops and evaluates forecasts, to determine actions required to maximize shareholder return. C...
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...
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,...
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...
We are currently looking for a talent to thrive in a client focused environment and join our Consulting team in Budapest.This opportunity knocks on the door of those who would like...
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 more complex projects.RESPONSIBILITIES Acts as a C...
Prepares and or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts...
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...