We are seeking a Regulatory Intelligence Associate Content Analyst to join our Life Sciences Regulatory Intelligence team in Barcelona.

You will contribute to Clarivate’s Cortellis Regulatory Intelligence database by monitoring global regulatory developments for medicinal products and medical devices.

In this role, you will track official regulatory updates, interpret new or revised requirements and ensure accurate, consistent country specific content within our AI enhanced editorial environment. A solid understanding of pharmaceutical and life sciences regulatory concepts, combined with strong analytical and research capabilities, is essential for success.

About You – experience, education, skills and accomplishments

At least one year of professional experience in the life sciences sector, ideally within a pharmaceutical company, CRO, biotechnology organisation, medical devices company or other regulated healthcare environment.Experience in regulatory or scientific writing, including interpreting legal or administrative texts and applying editorial standards, taxonomies and controlled vocabularies to structure and normalise regulatory information.Proficiency with digital workflow tools, content management systems and structured databases, including AI assisted editorial processes.Professional working proficiency in oral and written English.Advanced level of Spanish, German or Russian.

It would be great if you also had

Familiarity with content models, metadata and information architecture used for structuring regulatory intelligence.Experience using databases or structured information systems within global or distributed project teams.Experience checking content for accuracy and consistency and applying editorial standards, taxonomies and controlled vocabularies.Exposure to front end technologies or basic programming such as HTML, CSS or JavaScript, and familiarity with content models, metadata and information architecture.

What will you be doing in this role

Monitoring and collecting regulatory information from identified sources in line with CRI scope and editorial processes, compiling analyses and publishing regulatory documents.Gathering and analysing scientific, regulatory and industry data to support a comprehensive resource for the pharmaceutical and medical devices industry.Contributing to the development of regulatory content for the countries assigned within the Regulatory team.Creating harmonised content modules and standardised editorial content using established templates and taxonomies.

About the Team

You will report to the Senior Team Manager, Regulatory Information.You will be part of a team based in Barcelona, Paris, Belgrade, Penang and Hyderabad or Bangalore, collaborating remotely.We support leading pharmaceutical companies and healthcare organisations by providing the most up to date regulatory information to facilitate drug development and ensure safe access to the market.

Hours of Work

This is a permanent full time role at 40 hours per week (35 hours during July and August). The position is hybrid, requiring attendance at our Barcelona office, near Sagrada Familia, 2-3 times per week.

What We Can Offer

Active volunteering community with paid volunteering hoursPrivate health and life and disability insuranceTax free benefits, including Ticket Restaurant, kindergarten support and transport cardsGlobal and diverse employee base with more than forty nationalities30 working days of holiday

At Clarivate, we are committed to providing equal employment opportunities for all  qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.