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
IQVIA
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
The Role In this role youll be managing multiple large and complexglobal consulting projects for clients in the life science industry. This exciting opportunity will allow you to lead project teams to provide solutions to clients and identify further areas to support our clients to dr
The Role In this role youll be managing multiple large and complexglobal consulting projects for clients in the life science industry. This exciting opportunity will allow you to lead project teams to provide solutions to clients and identify further areas to support our clients to dr
Job OverviewProvide support and assistance to project managers and project teams related to the assigned project(s). Will support all project-related activities for assigned projects in accordance with SOPs policies and practices.Essential Functions Assist with the establishment of ne
Job OverviewProvide support and assistance to project managers and project teams related to the assigned project(s). Will support all project-related activities for assigned projects in accordance with SOPs policies and practices.Essential Functions Assist with the establishment of ne