Job OverviewReview & approve investigations, Root Cause Analysis (RCA), Corrective and Preventive Action (CAPA) and Effectiveness Check (EC) plans and track till closure for medium...
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 OverviewManage the execution of the assigned clinical study (ies) from initiation through to closeout. Ensure that clinical study management and project deliverables are on tim...
Job OverviewProvide leadership and advice on the development of optimum regulatory strategies for drug development, product lifecycle management and portfolio management, particula...
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...
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...
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...
Prepares and or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts...
Job Overview This position is for an Associate Quality Assurance Director in the Risk Analytics team who will serve as the strategic quality engagement leader focusing on risk anal...
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 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...
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 Consulting Services team helps pharmaceutical clients bring their products to market effectively and maintain an optimized promotional strategy through to product life cycle....
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...
The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territ...
Job OverviewAnalyses financial and business performance leveraging key indicators, develops and evaluates forecasts, to determine actions required to maximize shareholder return. C...
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...
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...
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...
Join us on our exciting journey!Our company. IQVIA. is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions ...
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...
Senior Site Manager Study Start Up with French languageReal World EvidenceHybrid Home based from different countries in EMEA.Join us on our exciting journey!IQVIA Real World Eviden...
Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and or international regulations, standard operatin...
Prepares and or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a C...
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...