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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.
Role overview
In this role within the EMEA RW MEG you will be producing materials and services relating to the Health Economics Outcomes Research business areas (health economic modelling, evide
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and comp
We are seeking an experienced Oncologist to support different expanding clinical trials in solid tumors, including the addition of new study arms. This role is fully focused on clinical trial support
We are seeking an experienced Oncologist to support different expanding clinical trials in solid tumors, including the addition of new study arms. This role is fully focused on clinical trial support
We are seeking an experienced Oncologist to support different expanding clinical trials in solid tumors, including the addition of new study arms. This role is fully focused on clinical trial support
The role participates in all aspects of the Medical Safety activities as per scope of work.
This includes, but is not limited to providing and maintaining of PV and risk management expertise to i
The role participates in all aspects of the Medical Safety activities as per scope of work.
This includes, but is not limited to providing and maintaining of PV and risk management expertise to i
The role participates in all aspects of the Medical Safety activities as per scope of work.
This includes, but is not limited to providing and maintaining of PV and risk management expertise to i
Job Overview:
As a Senior/Associate Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to meet internal and external
Provides data management support, oversight and/or accountability for one or more clinical trials.
Take the lead with the trial customer(s) and other internal and external partners to establish,
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
