IQVIA

Clinical Research Associate Trainee Program Auckland - Now taking applications for our next intake commencing on the 17th August 2026.Ready to kickstart your career in clinical research Join IQVIA a global leader in driving healthcare forward as a CRA Trainee! Were looking for critica

Clinical Research Associate Trainee Program Auckland - Now taking applications for our next intake commencing on the 17th August 2026.Ready to kickstart your career in clinical research Join IQVIA a global leader in driving healthcare forward as a CRA Trainee! Were looking for critica

Job OverviewOversee and direct the strategy and operational initiatives for the Enterprise Compliance Office. Provide advice on various areas of an effective compliance and ethics program. Ensure the compliance of IQVIA processes systems and projects with the applicable regulations gu

Job OverviewOversee and direct the strategy and operational initiatives for the Enterprise Compliance Office. Provide advice on various areas of an effective compliance and ethics program. Ensure the compliance of IQVIA processes systems and projects with the applicable regulations gu

Senior DevOps Engineer (Hybrid position)Throtle is seeking a motivated and enthusiastic Senior DevOps Engineer to join our growing technology team. You will play a crucial role in building deploying and maintaining our infrastructure and applications on Amazon Web Services (AWS). This

Senior DevOps Engineer (Hybrid position)Throtle is seeking a motivated and enthusiastic Senior DevOps Engineer to join our growing technology team. You will play a crucial role in building deploying and maintaining our infrastructure and applications on Amazon Web Services (AWS). This

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

Job OverviewProvide programming expertise to develop maintain and support programs that meet the needs of internal and external clients. Assist in leading the development of project-related solutions across a wide range of statistical programming activities.Essential FunctionsPlan per

Job OverviewProvide programming expertise to develop maintain and support programs that meet the needs of internal and external clients. Assist in leading the development of project-related solutions across a wide range of statistical programming activities.Essential FunctionsPlan per

Clinical Research Associate Trainee Program Melbourne - Now taking applications for our next intake commencing on the 17th August 2026.Ready to kickstart your career in clinical research Join IQVIA a global leader in driving healthcare forward as a CRA Trainee! Were looking for critic

Clinical Research Associate Trainee Program Melbourne - Now taking applications for our next intake commencing on the 17th August 2026.Ready to kickstart your career in clinical research Join IQVIA a global leader in driving healthcare forward as a CRA Trainee! Were looking for critic

Join us on our exciting journey!Position PurposeUnder guidance performs data analytics activities related to complex business problems and issues to provide insight to decision makers. May provide analytic support for internal project teams and for external client consulting or servic

Join us on our exciting journey!Position PurposeUnder guidance performs data analytics activities related to complex business problems and issues to provide insight to decision makers. May provide analytic support for internal project teams and for external client consulting or servic

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Please note: for this role you must be based in the Neth

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Please note: for this role you must be based in the Neth

OverviewIQVIA is looking for a Regulatory Affairs Consultant to join our Regulatory Affairs & Pharmacovigilance team in Italy. This role will support a range of client projects focused on the lifecycle management of medicinal products with opportunities to work on both local and inter

OverviewIQVIA is looking for a Regulatory Affairs Consultant to join our Regulatory Affairs & Pharmacovigilance team in Italy. This role will support a range of client projects focused on the lifecycle management of medicinal products with opportunities to work on both local and inter

JD for Performance/Automation QA Engineer 130General:Around 1-3 years of QA experienceAuthors and executes Performance and automation test cases for larger computer systems within the scope of a broader defined testing strategy.Ensures creation of test data to support test case execu

JD for Performance/Automation QA Engineer 130General:Around 1-3 years of QA experienceAuthors and executes Performance and automation test cases for larger computer systems within the scope of a broader defined testing strategy.Ensures creation of test data to support test case execu

Associate Project ManagerRole OverviewThe Associate Project Manager supports the Organizational Effectiveness (OE) team within US Operations working closely with Directorlevel OE Leads on initiatives such as organizational optimization location strategy thirdparty spend and change man

Associate Project ManagerRole OverviewThe Associate Project Manager supports the Organizational Effectiveness (OE) team within US Operations working closely with Directorlevel OE Leads on initiatives such as organizational optimization location strategy thirdparty spend and change man

Job OverviewAccountable for capability and learning activities related to the delivery of CDGM services and the adoption of TMF and good documentation practices across the business.ResponsibilitiesDevelop and implement effective fit-for-purpose capability development learning and know

Job OverviewAccountable for capability and learning activities related to the delivery of CDGM services and the adoption of TMF and good documentation practices across the business.ResponsibilitiesDevelop and implement effective fit-for-purpose capability development learning and know

Job OverviewThe Business Development Manager- MedTech is responsible for driving new and repeat business through strategic consultative sales efforts. This role focuses on building and maintaining relationships with key decisionmakers and influencers across both existing and prospecti

Job OverviewThe Business Development Manager- MedTech is responsible for driving new and repeat business through strategic consultative sales efforts. This role focuses on building and maintaining relationships with key decisionmakers and influencers across both existing and prospecti

Clinical Research Associate Your responsibilities will include:Performing site selection initiation monitoring and close-out visits after completing training periodSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accorda

Clinical Research Associate Your responsibilities will include:Performing site selection initiation monitoring and close-out visits after completing training periodSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accorda

The Clinical Study Report (CSR) Document Specialists is responsible to populate track QC and perform technical editorial checks of the CSR appendices for assigned studies from authoring until document finalization in the DMS in compliance with current Novartis processes ICH-GCP and re

The Clinical Study Report (CSR) Document Specialists is responsible to populate track QC and perform technical editorial checks of the CSR appendices for assigned studies from authoring until document finalization in the DMS in compliance with current Novartis processes ICH-GCP and re

Real World Evidence SolutionsRole OverviewTheAssociateDirector Solution and Delivery Lead (SDL) serves as a strategic scientific and delivery leader within Real World Evidence (RWE) Solutions. This role is accountable for shaping client strategy driving revenue growth and ensuring hig

Real World Evidence SolutionsRole OverviewTheAssociateDirector Solution and Delivery Lead (SDL) serves as a strategic scientific and delivery leader within Real World Evidence (RWE) Solutions. This role is accountable for shaping client strategy driving revenue growth and ensuring hig

Associate Director Product Strategy - IQVIA DigitalOverviewIQVIA is a global leader in advanced analytics technology solutions and clinical research dedicated to improving healthcare outcomes. Youll work alongside industry experts at the intersection of data science and decisionmaking

Associate Director Product Strategy - IQVIA DigitalOverviewIQVIA is a global leader in advanced analytics technology solutions and clinical research dedicated to improving healthcare outcomes. Youll work alongside industry experts at the intersection of data science and decisionmaking

Job OverviewThis role in IQVIAs Ethics and Compliance Office (ECO) focused on the Companys business in Europe and Latin America has two primary responsibilities. The incumbent: (1) is an Ethics and Compliance field team member handling the full range of ethics and compliance field mat

Job OverviewThis role in IQVIAs Ethics and Compliance Office (ECO) focused on the Companys business in Europe and Latin America has two primary responsibilities. The incumbent: (1) is an Ethics and Compliance field team member handling the full range of ethics and compliance field mat

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

Consultant Predictive Analytics IQVIA Inc. Wayne PA. May telecommute from anywhere in the U.S. with written business approval and report electronically to the Wayne PA office. Oversee advanced statistical/machine learning projects. Manage multiple work streams with data scientists dev

Consultant Predictive Analytics IQVIA Inc. Wayne PA. May telecommute from anywhere in the U.S. with written business approval and report electronically to the Wayne PA office. Oversee advanced statistical/machine learning projects. Manage multiple work streams with data scientists dev