Content Team Lead

hace 2 semanas

Madrid, España IQVIA A tiempo completo

We are looking for a passionate **Content Team Lead** for our** Regulatory Intelligence** area. 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**: - Lead and mange multi-regional team in - Monitoring new, revised or emerging regulatory requirements - Production of regulatory intelligence content and data framework - Engage with clients on regulatory content topics - Proactively lead and successfully complete the content development project: - Prioritize, scope and drive content creation - Contribute to the content identification and requirements and the content creation as well as supporting the QC of the content prior to launch. - Work in collaboration with the technical team to design and plan editorial processes and tools to maximize the delivery and quality to regulatory intelligence - Where additional support is required, work with external contractors - Act as a Regulatory Intelligence Lead on the cross-functional project team - Proactively engage with the team members, across direct line and dotted line of reporting, and bring the best of their performance by - Effective and result oriented goals and managing performance **Experience and Skills Required**: - Proven experience and tenures working in Regulatory Technology or Regulatory Intelligence within Life Sciences, preferably consultancy or industry, and with a minimum of 5 years of Regulatory experience and 2 years of experience in technology - Proven experience in managing and leading teams of Subject Matter Experts - Knowledge of quality management within Life Sciences - Demonstrated ability to manage and drive project contributions in a timely manner - Experience speaking and presenting to executives and leading business change - In-depth knowledge of IT systems used with regulatory, safety, clinical and quality (validated systems) - Experience in project and program management with creating roadmaps for the implementation of large-scale regulatory programs **We invite you to join IQVIA.** - IQVIA recognized by Great Place to Work as the second best company to work for in Spain (March 2018) - FORTUNE Magazine's World's Most Admired Companies list for the third year in a row. - Recognised 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.

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