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Mapa de ubicación: Madrid, Spain Full time R1317808

Descripción del trabajo

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.

This role will be defining the future data structure and subject matter requirements for this future content, as well as working with the technical teams on the implementation and will be responsible for forecasting, developing, and managing resource demand, and capacity planning to ensure the content elements of the project are completed on time to the required level of quality.

Principle Accountabilities:

To Accomplish this role, the candidate will have following responsibilities

  • 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

    • Mentoring, coaching and sharing subject matter expertise with others to elevate our capabilities to deliver world-class solutions for clients

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.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at

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