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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:
This unique role within IQVIA lends itself to a technically minded Project Manager with strong communication skills and SDTM knowledge. Having experience with SAS programming will
Job Overview
Provide Trial Master File (TMF) - Quality checks related assistance to study teams.
Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies,
Job Description
Key Responsibilities:
Achieving company sales targets for both base and growth
Build a highly motivated performing Key Accounts Management team
Tracking performance of
Job Description
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 part
Job Description
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 part
Job Overview:
As a Senior Site Activation Coordinator, under general supervision, you will perform tasks at a country level associated with site activation activities.
These activities will be
Job Description
Job Overview
Manage single and multi-service projects, ensuring quality deliverables on time, within budget and to the customer’s satisfaction; Provide expert skills as pa
Job Overview
Provide management and service delivery excellence of projects, as assigned by Clinical Event Validation and Adjudication (CEVA) management, covering single or multiple EAM (Endpoin
We are looking for a highly skilled and experienced Sr. Project Manager who will also serve as the Team Leader for our Project Managers. This role is pivotal in driving the success of our financial
Job Overview:
Support the Project Manager by attending meetings, preparing minutes and action logs, preparing protocol-specific laboratory instructions documents. Under supervision of the Projec
Job Description
Overview:
The Core Diabetes Model is a disease-simulation model used to inform health policy decisions and conduct economic evaluations for interventions aimed at controlling di
JOB OVERVIEW:
Under general supervision, designs, develops, and maintains the pipelines, infrastructure, tools, and frameworks needed to facilitate the collection, analysis,modelling and visuali
Job Description
IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical t
Job Description
IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical t
Job Description
Job Overview
Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within bud
Job Overview
Under broad guidance, designs or modifies database designs to solve database processing problems considering computer equipment capacity and limitations, operating time and form of
Job Description
The GDM will perform scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS).
Lookin
Job Description
Essential Functions :
Provides clinical registry support, oversight and/or accountability for one or more clinical trials.
Gathers content and integration requirements for reg
