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About IQVIA
Sharing a Vision to Drive Healthcare Forward
Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increa... read moresingly limited resources.
We are inspired by the potential and propelled by the possibilities. We share the vision to drive healthcare forward. To see how we can help accelerate progress and achievements. Others are developing these medical breakthroughs. We do our part by using breakthroughs in insights, technology and human intelligence to reimagine and deliver ways to help make them a reality.
It’s bigger than better clinical trials. Or advances in technologies and analytics. Or faster insights. It’s about exploring a new path to better health outcomes via Human Data Science. It’s about harnessing the power of the IQVIA COREâ„¢ to channel the insights, commercial and scientific depth, and executional expertise that drive maximum value for our customers.
Motivated by the industry we help, we’re committed to providing solutions that enable life sciences companies to innovate with confidence, maximize opportunities, and, ultimately, drive human health outcomes forward.
The Senior Contracts & Proposals Manager is responsible for coordinating and managing contracts, proposals, and other designated processes for assigned customers. This role ensures the del
This Clinical Data Team Lead will be responsible for managing end-to-end delivery of data management services for single/multi-service projects, ensuring quality deliverables on time and
This Clinical Data Team Lead will be responsible for managing end-to-end delivery of data management services for single/multi-service projects, ensuring quality deliverables on time and
Job Overview
The Senior Clinical Research Associate I (Sr CRA I) is responsible for monitoring and site management activities for asthma and respiratory clinical trials to ensure study conduct,
Review and provide input into all trial set-up documentation
Translate protocol and any applicable de-risking into the creation and maintenance of detailed technical specifications, mapping docum
Review and provide input into all trial set-up documentation
Translate protocol and any applicable de-risking into the creation and maintenance of detailed technical specifications, mapping docum
Our ever-growing Lifecycle Safety Medical team is expanding. We are hiring Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2) in Serbia, Croatia, Portugal, Hungary, Slovakia, Roma
Our ever-growing Lifecycle Safety Medical team is expanding. We are hiring Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2) in Serbia, Croatia, Portugal, Hungary, Slovakia, Roma
Our ever-growing Lifecycle Safety Medical team is expanding. We are hiring Pharmacovigilance Scientist 2 (Safety Aggregate Report Specialist 2) in Serbia, Croatia, Portugal, Hungary, Slovakia, Roma
Job Overview
Our ever-growing Lifecycle Safety Medical team is expanding. We are hiring Pharmacovigilance Scientist (Safety Aggregate Report Specialist) in Serbia, Croatia, Portugal, Hungary, Sl
Job Overview
Our ever-growing Lifecycle Safety Medical team is expanding. We are hiring Pharmacovigilance Scientist (Safety Aggregate Report Specialist) in Serbia, Croatia, Portugal, Hungary, Sl
Job Overview
Our ever-growing Lifecycle Safety Medical team is expanding. We are hiring Pharmacovigilance Scientist (Safety Aggregate Report Specialist) in Serbia, Croatia, Portugal, Hungary, Sl
This role is part of a sponsor dedicated project where you will be working with the client directly to manage deliveries.
The CMA contributes to the execution of the Centralized Monitoring proces
This role is part of a sponsor dedicated project where you will be working with the client directly to manage deliveries.
The CMA contributes to the execution of the Centralized Monitoring proces
This is an excellent opportunity to join a dynamic global business team responsible for developing budgets and proposals that support our Laboratory (IQVIA Laboratories) division.
Job Overview
The Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management to time
Job Overview
Project 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 Projec
Job Overview
Clinical Leads 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 C
