IQVIA

Regulatory & Start-Up Specialist 1IQVIA BiotechFranceHomebasedIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure collaborative culture and deep therapeutic expertise

Regulatory & Start-Up Specialist 1IQVIA BiotechFranceHomebasedIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure collaborative culture and deep therapeutic expertise

Job OverviewEnsures databases are up to date developed and supported to meet production requirements and that the production view is compatible with requirements and processes.Manages database enhancements; manages and consults on production views and provides direct support to refere

Job OverviewEnsures databases are up to date developed and supported to meet production requirements and that the production view is compatible with requirements and processes.Manages database enhancements; manages and consults on production views and provides direct support to refere

Job OverviewUnder broad guidance designs or modifies database designs to solve database processing problems considering computer equipment capacity and limitations operating time and form of desired results.Essential Functions Designs or modifies database designs to solve database pro

Job OverviewUnder broad guidance designs or modifies database designs to solve database processing problems considering computer equipment capacity and limitations operating time and form of desired results.Essential Functions Designs or modifies database designs to solve database pro

IQVIA Biotech is seeking CRA 2 candidates with a minimum of 1 year of on-site monitoring experience in internal medicine and/or neurology.IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligne

IQVIA Biotech is seeking CRA 2 candidates with a minimum of 1 year of on-site monitoring experience in internal medicine and/or neurology.IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligne

Role Purpose As the Sales Engineer you have a history of honing and exercising technical quantitative and commercial capabilities to achieve material business outcomes. You are obsessed with understanding a clients business and the best mechanism of extending a platform to help them m

Role Purpose As the Sales Engineer you have a history of honing and exercising technical quantitative and commercial capabilities to achieve material business outcomes. You are obsessed with understanding a clients business and the best mechanism of extending a platform to help them m

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordina

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordina

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

Role Purpose:Under close guidance or supervision responsible for monitoring data perform release operations and escalate to supervisorJob Description:Perform scheduled maintenance/release duties for US production.Solicits gathers and validates information from different sources to ide

Role Purpose:Under close guidance or supervision responsible for monitoring data perform release operations and escalate to supervisorJob Description:Perform scheduled maintenance/release duties for US production.Solicits gathers and validates information from different sources to ide

Job OverviewReview assess and process safety data and information across service lines received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under

Job OverviewReview assess and process safety data and information across service lines received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under

Job OverviewUnder broad guidance assists with the development and implementation of Service Management analytics and reporting solutions across multiple BI platforms (including Salesforce ServiceNow Power BI Tableau Spotfire Reportive and Snowflake). Delivers high-quality dashboards m

Job OverviewUnder broad guidance assists with the development and implementation of Service Management analytics and reporting solutions across multiple BI platforms (including Salesforce ServiceNow Power BI Tableau Spotfire Reportive and Snowflake). Delivers high-quality dashboards m

Job OverviewProvide Trial Master File (TMF) - Quality checks related assistance to study teams.Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs) policies practices good clinical practices applicable regulatory requirements and meets quality and timel

Job OverviewProvide Trial Master File (TMF) - Quality checks related assistance to study teams.Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs) policies practices good clinical practices applicable regulatory requirements and meets quality and timel

Safety Specialist FSP Team at IQVIAStep into a role where your attention to detail passion for patient safety and drive for excellence truly make an impact. The FSP team at IQVIA is looking for a dynamic Safety Specialist ready to grow collaborate and help deliver highquality pharmac

Safety Specialist FSP Team at IQVIAStep into a role where your attention to detail passion for patient safety and drive for excellence truly make an impact. The FSP team at IQVIA is looking for a dynamic Safety Specialist ready to grow collaborate and help deliver highquality pharmac

The Content Design Specialist must check content in various languages to ensure it does not contain any design error. He/she must track omission inaccuracy inconsistency and visibility errors coming from OCR translation and DTP tasks. It may entail correcting removing adding and forma

The Content Design Specialist must check content in various languages to ensure it does not contain any design error. He/she must track omission inaccuracy inconsistency and visibility errors coming from OCR translation and DTP tasks. It may entail correcting removing adding and forma

Director Data Platform ArchitectureAre you looking to make a difference and contribute to healthcare revolution If so this is a job for you!Who are weHuman Data Science company that accelerates innovation for healthier worldGlobal organization operating in over 100 countries hiring o

Director Data Platform ArchitectureAre you looking to make a difference and contribute to healthcare revolution If so this is a job for you!Who are weHuman Data Science company that accelerates innovation for healthier worldGlobal organization operating in over 100 countries hiring o

Job Overview: Under general supervision prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients. Provides regulatory support for assigned projects.Essential Functions:Acts as

Job Overview: Under general supervision prepares and/or reviews regulatory submissions documents to support clinical trial and marketing authorization activities for either internal and/or external clients. Provides regulatory support for assigned projects.Essential Functions:Acts as

Descripción de puestoEl delegado se responsabilizará de la información y promoción de los productos de la Compañía en su zona geográfica de influencia mejorando la experiencia del cliente identificando necesidades críticas y proporcionando soluciones óptimas para alcanzar los objetivo

Descripción de puestoEl delegado se responsabilizará de la información y promoción de los productos de la Compañía en su zona geográfica de influencia mejorando la experiencia del cliente identificando necesidades críticas y proporcionando soluciones óptimas para alcanzar los objetivo

This is an on-site position in Salt Lake City UtahOverview:This individual will play a key role in assisting in the conduct of clinical trial activities in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking

This is an on-site position in Salt Lake City UtahOverview:This individual will play a key role in assisting in the conduct of clinical trial activities in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking

As an HR Specialist you will support the continuous improvement of the HR function through development and implementation of HR programs in Argentina.With guidance provide HR support to employees and management across assigned service areas business units or departments.Provide suppor

As an HR Specialist you will support the continuous improvement of the HR function through development and implementation of HR programs in Argentina.With guidance provide HR support to employees and management across assigned service areas business units or departments.Provide suppor

Regulatory & Start Up Manager SpainIQVIA MedtechHomebasedJob OverviewDirect and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budge

Regulatory & Start Up Manager SpainIQVIA MedtechHomebasedJob OverviewDirect and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budge

ResponsibilitiesDelivers profitability and recognition for the organization by selling and providing services to customers utilizing organization tools techniques and intellectual capital to assist the healthcare industry by bettering processes implementing new technologies; and accru

ResponsibilitiesDelivers profitability and recognition for the organization by selling and providing services to customers utilizing organization tools techniques and intellectual capital to assist the healthcare industry by bettering processes implementing new technologies; and accru