Full Time

Looking for a role where your work truly matters Join IQVIAs Reference Data team and help shape the accuracy and integrity of healthcare data that drives global life sciences this remote position youll enjoy flexibility a collaborative team culture and the chance to build strong rela

Looking for a role where your work truly matters Join IQVIAs Reference Data team and help shape the accuracy and integrity of healthcare data that drives global life sciences this remote position youll enjoy flexibility a collaborative team culture and the chance to build strong rela

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Iqvia

Full Time

Position Summary:Care Managers are responsible for contacting insurance companies to obtain correct eligibility information perform benefit investigations copay assistance and check prior authorization and/ or appeal status.The information contained herein is intended to be an accurat

Position Summary:Care Managers are responsible for contacting insurance companies to obtain correct eligibility information perform benefit investigations copay assistance and check prior authorization and/ or appeal status.The information contained herein is intended to be an accurat

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Full Time

Clinical PharmacistType: Full-time hybrid (around 50% from home 50% at GP surgeries)We are looking for pharmacists to join the team to work across Bristol/ South WalesJoin us in this exciting role where you will utilise your clinical expertise and commercial acumen to support patients

Clinical PharmacistType: Full-time hybrid (around 50% from home 50% at GP surgeries)We are looking for pharmacists to join the team to work across Bristol/ South WalesJoin us in this exciting role where you will utilise your clinical expertise and commercial acumen to support patients

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Full Time

Clinical PharmacistType: Full-time hybrid (around 50% from home 50% at GP surgeries)We are looking for pharmacists to join the team to work across Dorset and HampshireJoin us in this exciting role where you will utilise your clinical expertise and commercial acumen to support patients

Clinical PharmacistType: Full-time hybrid (around 50% from home 50% at GP surgeries)We are looking for pharmacists to join the team to work across Dorset and HampshireJoin us in this exciting role where you will utilise your clinical expertise and commercial acumen to support patients

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Full Time

Job OverviewProvide Trial Master File (TMF) 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 timeline metrics.Ensu

Job OverviewProvide Trial Master File (TMF) 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 timeline metrics.Ensu

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The Translation Project Manager Linguistic Validation and eCOA is responsible for the development and harmonization of the Linguistic Validation and screenshot reviews of Clinical Outcome Assessments (COA) process within the IQVIA Translations team. Including but not limited to Patie

The Translation Project Manager Linguistic Validation and eCOA is responsible for the development and harmonization of the Linguistic Validation and screenshot reviews of Clinical Outcome Assessments (COA) process within the IQVIA Translations team. Including but not limited to Patie

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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 operations global or regional Quality Management team(s) f

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 operations global or regional Quality Management team(s) f

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The Part Time Clinical Consultant (PTCC) role is an exciting opportunity to join IQVIA. IQVIA/MedTech takes the approach to helping customers drive healthcare forward in this challenging fast-paced environment. We help customers accelerate results improve patient outcomes and unleash

The Part Time Clinical Consultant (PTCC) role is an exciting opportunity to join IQVIA. IQVIA/MedTech takes the approach to helping customers drive healthcare forward in this challenging fast-paced environment. We help customers accelerate results improve patient outcomes and unleash

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We are seeking a dynamic and results-driven professional with a proven track record of success in persuasion influence and negotiation. This role requires a strategic thinker who can increase share and recommendations among targeted healthcare professionals in Dermatology while effect

We are seeking a dynamic and results-driven professional with a proven track record of success in persuasion influence and negotiation. This role requires a strategic thinker who can increase share and recommendations among targeted healthcare professionals in Dermatology while effect

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IQVIA 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 allow us to deliver tailored solutions that help bring innovat

IQVIA 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 allow us to deliver tailored solutions that help bring innovat

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Full Time

We are seeking a Laboratory Assistant to join IQVIAs laboratory business at Valencia CA.Shift: Monday - Friday 8:30 AM - 5:00 PMWe hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purp

We are seeking a Laboratory Assistant to join IQVIAs laboratory business at Valencia CA.Shift: Monday - Friday 8:30 AM - 5:00 PMWe hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purp

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Company OverviewIQVIA is a leading global provider of research and development commercial solutions and technology-enabled services to the life sciences industry. We help customers accelerate innovation and improve patient outcomes by combining deep scientificexpertisewith advanced da

Company OverviewIQVIA is a leading global provider of research and development commercial solutions and technology-enabled services to the life sciences industry. We help customers accelerate innovation and improve patient outcomes by combining deep scientificexpertisewith advanced da

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Job Title:Research AssistantWork Set-Up:Working On-siteScheduled Weekly Hours:29 HoursJob Profile Summary: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 trial

Job Title:Research AssistantWork Set-Up:Working On-siteScheduled Weekly Hours:29 HoursJob Profile Summary: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 trial

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In partnership with our client we are actively searching for a Senior Key Account Representative to deliver on our commitment to serve patients. The specialty sales representative will be responsible for promoting a product to specialty healthcare providers in an assigned territory. T

In partnership with our client we are actively searching for a Senior Key Account Representative to deliver on our commitment to serve patients. The specialty sales representative will be responsible for promoting a product to specialty healthcare providers in an assigned territory. T

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Full Time

Job OverviewThe role involves comprehensive TMF review including crosscheck and co-dependency checks to ensure inspection readiness of TMF.Serve as the liaison between Records Management and user departments regarding Trial Master files. Apply Records Management expertise to provide p

Job OverviewThe role involves comprehensive TMF review including crosscheck and co-dependency checks to ensure inspection readiness of TMF.Serve as the liaison between Records Management and user departments regarding Trial Master files. Apply Records Management expertise to provide p

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As the only global provider of commercial solutions IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma medical device and diagnostic companies get their therapies to the people who need them. We help customers gain insight and access to

As the only global provider of commercial solutions IQVIA understands what it takes to deliver nationally and internationally. Our teams help biopharma medical device and diagnostic companies get their therapies to the people who need them. We help customers gain insight and access to

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Job Family DescriptionMonitors assigned sites to ensure that clinical research studies adhere to standard protocols and SOPs.Sub-Family DescriptionMonitors during clinical research studies to ensure trials are being conducted in accordance with widely accepted clinical practices.Condu

Job Family DescriptionMonitors assigned sites to ensure that clinical research studies adhere to standard protocols and SOPs.Sub-Family DescriptionMonitors during clinical research studies to ensure trials are being conducted in accordance with widely accepted clinical practices.Condu

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Full Time

Job OverviewServe as the liaison between Records Management and user departments regarding Trial Master files. Apply clinical research Records Management expertise to provide project related assistance across multiple project(s) sites and project teams. Ensure all work is conducted in

Job OverviewServe as the liaison between Records Management and user departments regarding Trial Master files. Apply clinical research Records Management expertise to provide project related assistance across multiple project(s) sites and project teams. Ensure all work is conducted in

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Full Time

About the RoleAs a Clinical Process Coordinator youll support clinical research projects by ensuring smooth processes and accurate documentation. This is an administrative role within our global team perfect for early-career professionals ready to learn and gradually grow their career

About the RoleAs a Clinical Process Coordinator youll support clinical research projects by ensuring smooth processes and accurate documentation. This is an administrative role within our global team perfect for early-career professionals ready to learn and gradually grow their career

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Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors studies or multi-protocol programs as determined by the Sponsors requirements.Essential Functions Develop Coordinate the development of investigator g

Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors studies or multi-protocol programs as determined by the Sponsors requirements.Essential Functions Develop Coordinate the development of investigator g

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