Medical Device Expert - Multiple European Locations

IQVIA ,
London, Greater London
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Overview

Job Description

Join us on our exciting journey! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. We are expanding the team in Tarius, part of the IQVIA's Global Market Insights (GMI) division. Tarius databases is an on-line, subscription based regulatory information provider to the global pharmaceutical and device industries, helping companies stay on top of Regulatory requirements. Tarius is IQVIAs on-line platform compiling reliable and up-to-date global regulatory information from more than 110 countries, regions, and international organizations. Tarius supports pharmaceutical and medical device companies by providing access to up to date and comprehensive original and translated regulatory documents, expert country summaries, tabulated comparative regulatory information covering operational details and timely alerts and state of the art functionality. Medical Device Expert to join an expanding team of content experts in Tarius (on-line platform). Your role You will join a dedicated and experienced team of senior regulatory experts who together with the Content Manager are responsible for the high quality regulatory content of the Database. In your role you will be responsible for the development of new content offerings within the Medical Device area working as part of the offering development projects on an on-going basis. As we are expanding the scope and improving the Medical Device information our offering as well as adding impact assessments, you are responsible for creating Medical Device intelligence content and insights of value to our customers. You will also be responsible for the on-going maintenance of Medical Device content in our offering. This includes the overall responsibility for the Medical Device regulatory content within Tarius as well as the Cross-Country Tables and Expert Summaries across all countries. You will succeed with this part of the role by collaboration with our local experts. As our Medical Device expert, you will be responsible for ensuring knowledge-sharing across the Tarius team on appropriate topics as well as establishing a network to other Medical Device experts in other parts of IQVIA. The team is based in Copenhagen but it is not required for you to work out of Copenhagen. Overview of Team The Medical Device expert will be joining an expanding team of senior regulatory experts who together with the content manager are responsible for the high quality regulatory content of the Database. The expert team is supported by a Global Network of Regulatory Experts consisting of more than 300 senior regulatory experts based worldwide. The local experts review and update information from their respective countries, providing their knowledge about local best practices and interpretation of the national regulations. In addition, the expert team works closely with the Multilingual Editorial Team, responsible for updating Tarius' online information database. Key Responsibilities * Drives the Medical Device content work in offering development projects expanding and improving the quality of the Medical Device regulatory content * Owns (in partnership with the content manager) the Medical Device regulatory content in Tarius including the relevant expert summaries and cross-country tables covering all countries * Responsible for ensuring the content quality standards are met at all times * Responsible for providing high-quality impact assessment of key regulatory documents EU and US * Collaborates with Local experts and Tarius Editorial Team on aspects related to the Medical Device regulatory content * Responsible for knowledge-sharing and training within the Medical Device regulatory area * May participate in client meetings as subject matter expert on the Medical Device regulatory content * Required Knowledge, Skills and Abilities * +5 years of experience within Medical Device regulatory area (preferably from device company or notified body) * In-depth knowledge on Medical Device regulations including: * Clinical trials in medical device development * Certification/marketing approvals * Packaging and labelling * Quality System requirements * Post-market surveillance and vigilance * Relevant ISO standards and others * Ability to assess impact of new regulatory requirements in EU and US * Master's degree or equivalent * Excellent English skills * Experience in working in a project setting * Knowledge of the medical device industry and its challenges * Business understanding/acumen * Ability to create strong working relationships across organisation (local experts, editors, consultants and external partners) Key Characteristics Proactive, Detail oriented, knowledgeable, consultative, problem

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