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Barcelona or Paris

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Job Title: Senior Editorial Analyst – Life Sciences

Department: Editorial
Business: IP & Science
Location: Barcelona or Paris
Conditions: 1 year temporary contract

Clarivate Analytics accelerates the pace of innovation by providing trusted insights and analytics to customers around the world, enabling them to discover, protect and commercialize new ideas faster. We own and operate a collection of leading subscription-based services focused on scientific and academic research, patent analytics and regulatory standards, pharmaceutical and biotech intelligence, trademark protection, domain brand protection and intellectual property management. Clarivate Analytics is now an independent company with over 4,000 employees, operating in more than 100 countries and owns well‐known brands that include Web of Science, Cortellis, Derwent, CompuMark, MarkMonitor and Techstreet, among others. For more information, visit

Today we are the established and authoritative pharmaceutical and biotechnology information resource, and the industry authority on the global generics market. Both innovators and generic manufacturers trust us because our integrated solutions contain an unrivalled breadth and depth of timely, relevant strategic information from multiple databases, delivered on powerful platforms, accompanied by intuitive analytical tools, and backed up by dedicated support teams.

But we provide far more than just content sets. Our data are enriched with unique abstracts, commentaries and analysis prepared by our team of industry experts — critical insight on-tap from the thought leaders that shape pharmaceutical opinion. All over the world, decision-makers depend on us for the essential knowledge that can justify their strategies, promote outstanding research and business growth, and keep them abreast of the market.

Main Purpose of Job:

Regulatory Drug information is part of the Clarivate Analytics IP and Science Editorial Operations Group and comprises several teams responsible for the daily collection, synthesis and maintenance of data relating to regulatory information. These records form a core element of our Cortellis RI database.
The main role of the Editorial Analyst involves collecting regulatory information, compiling analyses, publishing the regulatory documents. He/she gathers and analyses a variety of scientific, regulatory and industry data to provide a comprehensive resource for the Pharmaceutical industry.
Within the European team, the candidate will participate to the elaboration and development of the regulatory content for the EU modules assigned.


1. Research news releases and other information sources
2. Analysis of news alerts and researched articles on current pharmaceutical markets
3. Editing all copies to a high standard for publication
4. Update the Cortellis RI database
5. Take in charge analysis of regulatory information under the supervision of the country manager
6. Manage update of contracts, invoices etc in link with editorial activity
7. Undertake any other reasonable duties as requested by the line manager on a permanent or temporary basis

Skills / Experience:

• Ability to research and synthesis complex data and information
• Advanced level of English
• A good team player with the ability to work on own initiative
• Computer literacy, preferably with some database experience
• Good eye for detail
• Problem identification and solving skills
• Excellent time management
• Ability to work in a global team

• Good command of any other European language
• Editing and proofreading experience
• Background in life sciences much appreciated
• Understanding of the pharmaceutical/medical device industry and its key commercial drivers


• Communication/Editorial/Linguistic
• 3 years of working experience minimum

CVs should be sent to Maria Nicolau at

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