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We are looking for a passionate **Subject Matter Expert** for our Regulatory Intelligence area. As the regulatory **Subject Matter Expert**, you will collaborate closely with a broad network of internal and external specialists working on active project delivery. You will also be leading the on-going creation and quality management of the future regulatory content. This role will involve actively interacting with customers to discuss The **IQVIA Regulatory Intelligence** service provides the pharmaceutical and medical device industries easy access to original and translated regulatory documents, summarized regulatory intelligence and comparative tables with up-to-date key regulatory requirements worldwide. As we look to develop our Regulatory offering further, this role is to be part of the team designing for the future of Regulatory Intelligence. **Principle Accountabilities**: - Subject matter expert (SME) in Regulatory submissions - Proactively drive and successfully complete this future content development project by: - Monitoring new, revised or emerging regulatory requirements - Contributing to the content identification and requirements and the content creation as well as supporting the QC of the content prior to launch. **Experience and Skills Required**: - Qualifications in life sciences or related discipline - Subject matter expert (SME) in Regulatory submissions eg - Chemistry, Manufacturing and Controls, - Variations - New product registrations - Demonstrated ability to manage and drive project contributions in a timely manner **We invite you to join IQVIA**: - Recognized by **Great Place to Work** as the second best company to work for in Spain (March 2019) - ** FORTUNE Magazine's World's Most Admired Companies** list for the third year in a row (January 2020) - Recognized by the 2016 Scrip Awards as the **Best Full-service Provider Contract Research Organization** (CRO) - Awarded the 2016 Eagle Award from the Society for Clinical Research Sites (SCRS) for the fourth consecutive year. - A site-nominated award recognizing contract research organizations (CRO) and biopharmaceutical sponsors dedicated to **building positive relationships with research sites through leadership, professionalism and integrity**. - IQVIA named in The International Association of Outsourcing Professionals (IAOP) 2017 Global Outsourcing 100® List which recognizes the world’s best service providers across a range of industries. IQVIA is an **equal opportunity employer**. We make employment decisions based on qualifications and merit. We prohibit discrimination based on any unlawful consideration such as age, race, national origin, gender or other "protected status.“ **If you're not a EU citizen you must have a resident visa or a permanent visa.
