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

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

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

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

Tu impactoDiseñar e implementar el plan de marketing anual de la línea alineando objetivos canales y métricas de éxito.Definir posicionamiento mensajes clave y propuesta de valor asegurando relevancia clínica y diferenciación competitiva.Analizar mercado competencia y tendencias para

Tu impactoDiseñar e implementar el plan de marketing anual de la línea alineando objetivos canales y métricas de éxito.Definir posicionamiento mensajes clave y propuesta de valor asegurando relevancia clínica y diferenciación competitiva.Analizar mercado competencia y tendencias para

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 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

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

The DTP Team Lead is responsible for leading a team of Content Design Specialists who ensure translation projects are delivered according to IQVIAs standards and design requirements. He/she builds and maintains strong relationships within his/her team with Project Managers as well as

The DTP Team Lead is responsible for leading a team of Content Design Specialists who ensure translation projects are delivered according to IQVIAs standards and design requirements. He/she builds and maintains strong relationships within his/her team with Project Managers as well as

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

We are seeking aresilient strategic and self-driven Key Account Manager(m/f/d) in Germany to further expand our footprint in theCardioplegia marketthrough aclient-dedicated role. You will be responsible for driving the customer journey experience in hospitals that undergo open-heart s

We are seeking aresilient strategic and self-driven Key Account Manager(m/f/d) in Germany to further expand our footprint in theCardioplegia marketthrough aclient-dedicated role. You will be responsible for driving the customer journey experience in hospitals that undergo open-heart s

The IQVIA Sponsor-Dedicated Clinical Trials Assistant Team issupporting the project teams in the execution of clinical the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved i

The IQVIA Sponsor-Dedicated Clinical Trials Assistant Team issupporting the project teams in the execution of clinical the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved i

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

Project Role: Programmer Analyst or Software Devl Analyst 2Work Experience: 2 to 8 yearsWork Mode: HybridMust Have Skills: Veeva CDMS or Veeva CDBJob Roles & Responsibilities:Veeva CDMS -Veeva Vault CDMS knowledge: Deep understanding of Vault EDC Vault Coder and Vault DataWorkbench.CD

Project Role: Programmer Analyst or Software Devl Analyst 2Work Experience: 2 to 8 yearsWork Mode: HybridMust Have Skills: Veeva CDMS or Veeva CDBJob Roles & Responsibilities:Veeva CDMS -Veeva Vault CDMS knowledge: Deep understanding of Vault EDC Vault Coder and Vault DataWorkbench.CD

Job OverviewUnder direct supervision assist with the development and preparation of pharmacovigilance agreements for assigned customers.Essential Functions Under direct supervision work closely with project team to determine appropriate terms and conditions of safety agreements. Under

Job OverviewUnder direct supervision assist with the development and preparation of pharmacovigilance agreements for assigned customers.Essential Functions Under direct supervision work closely with project team to determine appropriate terms and conditions of safety agreements. Under

Senior Site Activation Coordinator ICF (Informed Consent Form)Locations: Bulgaria South Africa Slovakia SerbiaWork Model: HybridMake an impact on patient health with IQVIA!Join our Global Site Activation Team a 2000strong network driving highquality site activation and ensuring pa

Senior Site Activation Coordinator ICF (Informed Consent Form)Locations: Bulgaria South Africa Slovakia SerbiaWork Model: HybridMake an impact on patient health with IQVIA!Join our Global Site Activation Team a 2000strong network driving highquality site activation and ensuring pa

IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client envir

IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client envir

Location: Guatemala City Work Type: HybridAbout the RoleJoin our team as a Business Intelligence Analyst where you will be responsible for data investigation query resolution data transformations and delivering valuable insights to the business. This role supports internal stakeholder

Location: Guatemala City Work Type: HybridAbout the RoleJoin our team as a Business Intelligence Analyst where you will be responsible for data investigation query resolution data transformations and delivering valuable insights to the business. This role supports internal stakeholder

Job OverviewClinical Trial Manager are an integral part of clinical trial delivery working alongside clinical teams to improve patients lives by bringing new drugs to the market faster. The Clinical Trial manager is a member of the core project team responsible for the clinical delive

Job OverviewClinical Trial Manager are an integral part of clinical trial delivery working alongside clinical teams to improve patients lives by bringing new drugs to the market faster. The Clinical Trial manager is a member of the core project team responsible for the clinical delive