IQVIA

Looking for a Product Specialist oncologists.#LI-CES #LI-DNPIQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development

Looking for a Product Specialist oncologists.#LI-CES #LI-DNPIQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development

Job OverviewProvides administrative and/or technical support.Essential Functions Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors studies as well as reconcile the total GPS Sponsor balance to the Corporate Sponsor Balance on a month

Job OverviewProvides administrative and/or technical support.Essential Functions Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors studies as well as reconcile the total GPS Sponsor balance to the Corporate Sponsor Balance on a month

Job OverviewUnder close guidance or supervision bridges and codes data into IQVIA systems.Essential Functions Develops an understanding of the technical knowledge needed to code and bridge data. Completes basic coding and bridging of data referring non-routine matter to more experienc

Job OverviewUnder close guidance or supervision bridges and codes data into IQVIA systems.Essential Functions Develops an understanding of the technical knowledge needed to code and bridge data. Completes basic coding and bridging of data referring non-routine matter to more experienc

The main purpose of this role is to write the requirements of the assigned IRT studies and manage the implementation in a way that ensures all patients get treated with the right study drug as per the Sponsors study protocol. This is a highly consultative position in which the PM need

The main purpose of this role is to write the requirements of the assigned IRT studies and manage the implementation in a way that ensures all patients get treated with the right study drug as per the Sponsors study protocol. This is a highly consultative position in which the PM need

To be eligible for this position you must reside in the same country where the job is located.IQVIA is The Human Data Science Company focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that har

To be eligible for this position you must reside in the same country where the job is located.IQVIA is The Human Data Science Company focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions that har

The Business Development Manager works collaboratively with internal and external colleagues to increase sales within the Data Sciences Staffing Team specifically in the disciplines of Clinical Data Management Biostatistics and Statistical Programming.Responsibilities include full cyc

The Business Development Manager works collaboratively with internal and external colleagues to increase sales within the Data Sciences Staffing Team specifically in the disciplines of Clinical Data Management Biostatistics and Statistical Programming.Responsibilities include full cyc

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together we support innovation from concept to commercialization offering expertise in regulatory strateg

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together we support innovation from concept to commercialization offering expertise in regulatory strateg

Job OverviewAs a senior member of IQVIAs Global Advisory Services team you will work directly with Global HQ Pharma clients as a trusted partner helping them navigate complex strategic technological and operational challenges. You will shape and deliver highimpact consulting engagemen

Job OverviewAs a senior member of IQVIAs Global Advisory Services team you will work directly with Global HQ Pharma clients as a trusted partner helping them navigate complex strategic technological and operational challenges. You will shape and deliver highimpact consulting engagemen

Role Overview:The Technical Consultant will serve as a strategic advisor and technical expert supporting the clients initiatives within the nphies ecosystem. This role demands a deep understanding of healthcare interoperability standards particularly FHIR (Fast Healthcare Interoperabi

Role Overview:The Technical Consultant will serve as a strategic advisor and technical expert supporting the clients initiatives within the nphies ecosystem. This role demands a deep understanding of healthcare interoperability standards particularly FHIR (Fast Healthcare Interoperabi

requested. The Associate Medical Safety Director participates in all aspects of Medical Safetys involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors.Essential Functions Perform medical review

requested. The Associate Medical Safety Director participates in all aspects of Medical Safetys involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors.Essential Functions Perform medical review

IQVIA Biotech Is Hiring experienced Clinical Research Associates (Central Poland)Join IQVIA today and make an impact on patients outcome!Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by t

IQVIA Biotech Is Hiring experienced Clinical Research Associates (Central Poland)Join IQVIA today and make an impact on patients outcome!Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by t

Clinical Research Nurse - Malmö part time 24h per weekStart Date: ImmediateDuration: Approximately 6 monthsIQVIA is currently recruiting a dedicated Clinical Research Nurse to support a clinical research site in Malmö. This part-time position offers a unique opportunity to contribute

Clinical Research Nurse - Malmö part time 24h per weekStart Date: ImmediateDuration: Approximately 6 monthsIQVIA is currently recruiting a dedicated Clinical Research Nurse to support a clinical research site in Malmö. This part-time position offers a unique opportunity to contribute

Job OverviewThis role is an individual contributor assigned to designated Delivery Unit(s) sponsor(s) business line(s) and/or specific tasks as defined by the line manager (LM). The purpose of this role is to work together with global or regional Quality Management team(s) functional

Job OverviewThis role is an individual contributor assigned to designated Delivery Unit(s) sponsor(s) business line(s) and/or specific tasks as defined by the line manager (LM). The purpose of this role is to work together with global or regional Quality Management team(s) functional

Buscamos 1 Delegad@ de Visita Hospitalaria para realizar visitas a traumatólogicos medicos de urgencia y de medicina interna.Tu trabajo consistirá en la promoción de los productos en los hospitales asignados dentro de tu zona de trabajo contribuyendo así al plan de negocio nacional.El

Buscamos 1 Delegad@ de Visita Hospitalaria para realizar visitas a traumatólogicos medicos de urgencia y de medicina interna.Tu trabajo consistirá en la promoción de los productos en los hospitales asignados dentro de tu zona de trabajo contribuyendo así al plan de negocio nacional.El

Job Responsibilities:Complete maintenance of reference data (healthcare Organizations and Prescribers) as essential for ANZ Production.Perform research such as Internet Search Phone Verification Database Matches and etc. to gather information from third parties that will validate the

Job Responsibilities:Complete maintenance of reference data (healthcare Organizations and Prescribers) as essential for ANZ Production.Perform research such as Internet Search Phone Verification Database Matches and etc. to gather information from third parties that will validate the

Responsibilities: Recreate user problems to resolve operating difficulties and recommend system modifications to reduce user problems. Escalate more complex problems to appropriate level of management and provide information on problems that are severe in nature or that are exceeding

Responsibilities: Recreate user problems to resolve operating difficulties and recommend system modifications to reduce user problems. Escalate more complex problems to appropriate level of management and provide information on problems that are severe in nature or that are exceeding

Job Summary Under the direction and supervision of the Assistant Director of Clinical Trial Management this position is responsible for all serious adverse event (SAE) reporting SAE record requests and SAE data entry. The position works closely with the NEXT Investigators at all NEXT

Job Summary Under the direction and supervision of the Assistant Director of Clinical Trial Management this position is responsible for all serious adverse event (SAE) reporting SAE record requests and SAE data entry. The position works closely with the NEXT Investigators at all NEXT

Job OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to

Job OverviewManage end-to-end delivery of data management services for single/multi-service projects with minimal guidance ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to

requested. The Associate Medical Safety Director participates in all aspects of Medical Safetys involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors.Essential Functions Perform medical review

requested. The Associate Medical Safety Director participates in all aspects of Medical Safetys involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors.Essential Functions Perform medical review

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenanc

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenanc