IQVIA

Job OverviewProvides high quality timely development and on-time input to solutions for service delivery managed services or implementation oriented client projects. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex

Job OverviewProvides high quality timely development and on-time input to solutions for service delivery managed services or implementation oriented client projects. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex

About UsAt IQVIA our Nordic public health team collaborates closely with clients to co-develop data-driven solutions that enhance patient outcomes and deliver tangible value to the healthcare sector. We possess in-depth knowledge of health data and technology as well as a thorough und

About UsAt IQVIA our Nordic public health team collaborates closely with clients to co-develop data-driven solutions that enhance patient outcomes and deliver tangible value to the healthcare sector. We possess in-depth knowledge of health data and technology as well as a thorough und

Job OverviewSupport the continuous improvement of the staffing function through development and implementation for all staffing programs in an assigned business unit/department primarily in one geography. May be required to assist with providing staffing support to assigned management

Job OverviewSupport the continuous improvement of the staffing function through development and implementation for all staffing programs in an assigned business unit/department primarily in one geography. May be required to assist with providing staffing support to assigned management

Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Sta

Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Sta

Job OverviewThis is staff position within the Data Management Group providing support of customer EDI and flat file data processing functions. This position involves monitoring data processing systems EDI transaction flow and providing error resolution. This position is also responsib

Job OverviewThis is staff position within the Data Management Group providing support of customer EDI and flat file data processing functions. This position involves monitoring data processing systems EDI transaction flow and providing error resolution. This position is also responsib

Site Research Assistant Nijmegen (Part-Time 24 hours/week)Start Date: immediatelyDuration: Approximately 6 monthsIQVIA is currently recruiting a dedicated Site Research Assistant to support a clinical research site in Nijmegen. This part-time position offers a unique opportunity to c

Site Research Assistant Nijmegen (Part-Time 24 hours/week)Start Date: immediatelyDuration: Approximately 6 monthsIQVIA is currently recruiting a dedicated Site Research Assistant to support a clinical research site in Nijmegen. This part-time position offers a unique opportunity to c

Join a great team of young & smart talents!Reporting to the Belux Finance Manager the role will support all Financial Planning & Analysis aspects of the Commercial Solutions business in Belgium and Luxembourg.Tasks and responsibilitiesWhat Youll Do: Reporting & provide control coordin

Join a great team of young & smart talents!Reporting to the Belux Finance Manager the role will support all Financial Planning & Analysis aspects of the Commercial Solutions business in Belgium and Luxembourg.Tasks and responsibilitiesWhat Youll Do: Reporting & provide control coordin

Essential Functions Interpret clinical trial protocols to create and execute an effective clinical trial supply chain solution Create master English label text in accordance with relevant regulatory framework (e.g. Annex 13) Create and maintain demand forecasts and packaging plans so

Essential Functions Interpret clinical trial protocols to create and execute an effective clinical trial supply chain solution Create master English label text in accordance with relevant regulatory framework (e.g. Annex 13) Create and maintain demand forecasts and packaging plans so

Job OverviewProvides high quality timely development and on-time input to client solutions for the pharmaceutical and related industries.Assignments typically require basic analysis and problem solving.Essential Functions Under direct supervision assists with the review and analysis o

Job OverviewProvides high quality timely development and on-time input to client solutions for the pharmaceutical and related industries.Assignments typically require basic analysis and problem solving.Essential Functions Under direct supervision assists with the review and analysis o

JOB OVERVIEWThis position forms part of the Lead Contract Negotiators (LCN) - which supports the organizations agreements globally. The successful candidate will primarily focus on Software-as-a-Service (SaaS) agreements for IQVIA Technologies and will be expected to handle an extensi

JOB OVERVIEWThis position forms part of the Lead Contract Negotiators (LCN) - which supports the organizations agreements globally. The successful candidate will primarily focus on Software-as-a-Service (SaaS) agreements for IQVIA Technologies and will be expected to handle an extensi

Job Overview:The Site Activation Coordinator is responsible for supporting and coordinating all activities related to the activation of clinical trial sites from site selection through site initiation. The role ensures that sites are activated efficiently compliantly and on timeline b

Job Overview:The Site Activation Coordinator is responsible for supporting and coordinating all activities related to the activation of clinical trial sites from site selection through site initiation. The role ensures that sites are activated efficiently compliantly and on timeline b

Full-time 100% home-based roleJob OverviewReview structured clinical patient data output without direct access to medical charts to ensure medical plausibility and determine adherence to protocol and overall completeness and readiness of the supplied patient information for next level

Full-time 100% home-based roleJob OverviewReview structured clinical patient data output without direct access to medical charts to ensure medical plausibility and determine adherence to protocol and overall completeness and readiness of the supplied patient information for next level

Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Sta

Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Sta

Job OverviewSupport the continuous improvement of the staffing function through development and implementation for all staffing programs in an assigned business unit/department primarily in one geography. May be required to assist with providing staffing support to assigned management

Job OverviewSupport the continuous improvement of the staffing function through development and implementation for all staffing programs in an assigned business unit/department primarily in one geography. May be required to assist with providing staffing support to assigned management

Base level rolePerform comprehensive data management tasks including data review query generation and query resolution. This may also include but is not limited to creation of eCRF completion guidelines entry of test data for eCRF and the Data Review Model testing of data validation r

Base level rolePerform comprehensive data management tasks including data review query generation and query resolution. This may also include but is not limited to creation of eCRF completion guidelines entry of test data for eCRF and the Data Review Model testing of data validation r

IQVIA is recruiting a Regional Sales Manager to lead commercial activity for a portfolio of specialty medicines on behalf of one of our pharmaceutical partners. This role provides the opportunity to take responsibility for multiple countries operating within a complex matrix environme

IQVIA is recruiting a Regional Sales Manager to lead commercial activity for a portfolio of specialty medicines on behalf of one of our pharmaceutical partners. This role provides the opportunity to take responsibility for multiple countries operating within a complex matrix environme

IQVIA is recruiting Specialty Sales Representatives on behalf of one of our pharmaceutical partners to support the promotion of a portfolio of specialty medicines within specialist healthcare settings.These roles focus on highquality compliant engagement with healthcare professionals

IQVIA is recruiting Specialty Sales Representatives on behalf of one of our pharmaceutical partners to support the promotion of a portfolio of specialty medicines within specialist healthcare settings.These roles focus on highquality compliant engagement with healthcare professionals

Site Management Intern Job DescriptionA great opportunity for students eager to begin a career in Clinical Research and gain handson exposure to the work of Clinical Research Associates (CRAs) and Clinical Trial Assistants (CTAs).Key ResponsibilitiesTraining & OnboardingParticipate i

Site Management Intern Job DescriptionA great opportunity for students eager to begin a career in Clinical Research and gain handson exposure to the work of Clinical Research Associates (CRAs) and Clinical Trial Assistants (CTAs).Key ResponsibilitiesTraining & OnboardingParticipate i

Intern - IQVIALocation: Paddington LondonDuration of Internship: 11th May26 - 31st July26Job OverviewProvides administrative and/or technical support.Role & ResponsibilitiesShadow members of the consulting and account management teamsConduct structured market company and desk research

Intern - IQVIALocation: Paddington LondonDuration of Internship: 11th May26 - 31st July26Job OverviewProvides administrative and/or technical support.Role & ResponsibilitiesShadow members of the consulting and account management teamsConduct structured market company and desk research

Project Manager roleLocation: Leeds UK (Hybrid role)Job OverviewTo manage and maintain all operational aspects of projects being delivered by the business. To work closely with clients to ensure their needs are met and that the project meet desired outcomes within budget and scope. Wi

Project Manager roleLocation: Leeds UK (Hybrid role)Job OverviewTo manage and maintain all operational aspects of projects being delivered by the business. To work closely with clients to ensure their needs are met and that the project meet desired outcomes within budget and scope. Wi