Job OverviewProvide support for continuous improvement of the compensation/benefits function through development and implementation of all compensation/benefits programs in assigned region and business line. Provide expertise support and consultation on compensation/benefits matters e
Job OverviewProvide support for continuous improvement of the compensation/benefits function through development and implementation of all compensation/benefits programs in assigned region and business line. Provide expertise support and consultation on compensation/benefits matters e
Location: Remote candidates must be US-basedJoin IQVIAs Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient
Location: Remote candidates must be US-basedJoin IQVIAs Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient
Iqvia
Job OverviewAssists with the design/development of software solutions requiring general domain knowledge and limited business expertise.Troubleshoots code issues and continuously evolves IQVIAs platforms to meet user requirements/needs.Essential Functions Assists with the design/devel
Job OverviewAssists with the design/development of software solutions requiring general domain knowledge and limited business expertise.Troubleshoots code issues and continuously evolves IQVIAs platforms to meet user requirements/needs.Essential Functions Assists with the design/devel
Iqvia
Grade 160 Associate Director部署チーム名 LCSLifecycle Safety安全性部門Safety Operationsチームをリードしグローバルおよびローカルの基準に沿った業務運営を推進いただきます社内外の関係者と連携しながらプロジェクトの品質納期コスト管理を担い顧客への高品質なサービス提供と事業成長に貢献いただくポジションです部署チーム紹介LCSLifecycle Safetyは臨床試験から市販後に至るまで医薬品のライフサイクル全体にわたる安全性情報管理サービスを提供する部門です本ポジションが所属するSafety Project
Grade 160 Associate Director部署チーム名 LCSLifecycle Safety安全性部門Safety Operationsチームをリードしグローバルおよびローカルの基準に沿った業務運営を推進いただきます社内外の関係者と連携しながらプロジェクトの品質納期コスト管理を担い顧客への高品質なサービス提供と事業成長に貢献いただくポジションです部署チーム紹介LCSLifecycle Safetyは臨床試験から市販後に至るまで医薬品のライフサイクル全体にわたる安全性情報管理サービスを提供する部門です本ポジションが所属するSafety Project
Iqvia
Job OverviewProject Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical st
Job OverviewProject Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical st
Location: Remote candidates must be US-basedJoin IQVIAs Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient
Location: Remote candidates must be US-basedJoin IQVIAs Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient
Location: Remote candidates must be US-basedJoin IQVIAs Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient
Location: Remote candidates must be US-basedJoin IQVIAs Sponsor-Dedicated FSP team and help advance healthcare through real-world evidence. We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.We are seeking a Canada-based Senior Clini
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.We are seeking a Canada-based Senior Clini
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
Our MedTech Field Service Technician experiences a unique opportunity employ their technical experience by collaborating with healthcare professionals and leading technical initiatives in medical device technology. You will be responsible for troubleshooting repairing and updating med
Our MedTech Field Service Technician experiences a unique opportunity employ their technical experience by collaborating with healthcare professionals and leading technical initiatives in medical device technology. You will be responsible for troubleshooting repairing and updating med
JD Software QA Engineer 1 (130)Roles & ResponsibilitiesCollaborate closely with crossfunctional teams to analyze understand and clarify business and system requirements.Review functional requirements specifications and technical design documents to derive effective test coverage.Desi
JD Software QA Engineer 1 (130)Roles & ResponsibilitiesCollaborate closely with crossfunctional teams to analyze understand and clarify business and system requirements.Review functional requirements specifications and technical design documents to derive effective test coverage.Desi
To be eligible for this position you must reside in the same country where the job is located. Job Summary:Contribute to the growth and development of the IQVIA MedTech Strategy Consulting organization. We are investing across the board to provide Concept to Market capabilities to our
To be eligible for this position you must reside in the same country where the job is located. Job Summary:Contribute to the growth and development of the IQVIA MedTech Strategy Consulting organization. We are investing across the board to provide Concept to Market capabilities to our
Iqvia
Job OverviewUnder broad guidance ensures clients obtain maximum value from products and services in order to facilitate a positive and productive long-term relationship either broad client or offering focused.Essential Functions Ensures fulfillment of contract specifications and ad-ho
Job OverviewUnder broad guidance ensures clients obtain maximum value from products and services in order to facilitate a positive and productive long-term relationship either broad client or offering focused.Essential Functions Ensures fulfillment of contract specifications and ad-ho
IQVIA is expanding its team and is seeking a Market Access Manager based inFrance. This is one of several newly created roles across the EU due to our customers ongoing success and ahead of product launches in 2026.Our customer is a global biopharmaceutical company dedicated to bringi
IQVIA is expanding its team and is seeking a Market Access Manager based inFrance. This is one of several newly created roles across the EU due to our customers ongoing success and ahead of product launches in 2026.Our customer is a global biopharmaceutical company dedicated to bringi
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
The IQVIA Internship provides you with the opportunity to gain relevant project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact your future.You will be wo
The IQVIA Internship provides you with the opportunity to gain relevant project-based work experience at one of the most successful and cutting-edge global clinical research units in the market while building relationships within the company that will impact your future.You will be wo
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
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
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.We are seeking a US-based Senior Project M
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.We are seeking a US-based Senior Project 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