Job Overview
Manages activities to create global reference data and/or researches and analyses data components for more complex data projects, data standards, quality assurance work and client queries.
Essential Functions
• Performs a combination of any of the following: Schedules and leads day-to-day creation of global data elements.
• Manages teams to create global data elements.
• Recommends and implements local improvements to work processes; provide input to system developments.
• Carries out in depth research and analyses on global data for projects, data standards creation, quality assurance activities, client queries.
• Manages quality assurance and data standards activities.
Qualifications
• Bachelor's Degree or equivalent, in biomedical subject Req
• Five (5) years’ relevant experience in pharmaceutical information/data creation environment. Req
• In-depth knowledge of global pharmaceutical information in a variety of areas, as well as detailed knowledge of how data is integrated in global client offerings.
• Good organizational and analytical skills.
• Good understanding of global offerings and global data in IQVIA.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
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 complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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