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Barcelona or Paris

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Job Title: Managing Editor Regulatory Intelligence

Department: Life Sciences
Business: Life Sciences
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.

Job description :
You will work within the Life Science regulatory editorial team with primary responsibility for:

1/ Regulatory surveillance for a given set of European countries

 Driving the maintenance of content for a set of the Cortellis Regulatory Intelligence (CRI) European country modules by interacting with local consultants and regulatory Agencies.
 Monitoring changes and evolution of local regulatory landscape for both drug and medical devices.
 Analyzing the impact of drug/devices changing regulations to create and /or enrich CRI proprietary documents.
 Monitoring agency and professional websites, local specialized press, conferences selecting documents to be integrated in line with CRI Scope and editorial processes

2/ Development of new regulatory content
- Take in charge development of new content for EU countries for drug and/or medical device content
- Coordinate cross countries validation of content.

3/ Administrative tasks

Management of contract with local consultants and Health Agency, investigation and negotiate copyrights, responsibility, follow-up and control of budget per module

4/ Customers/Sales support

Provide customer support and expertise; communicate new regulatory content to sales or product specialists.

Required skills / Experience:
• Scientific degree in chemistry, pharmacology, biology
• At least 5 years of working experience in Regulatory Affairs
• Fluent in English, another European language will be much appreciated
• Good problem solver and able to demonstrate good judgment in decision making and setting priorities.
• Capability to work remotely with peers in an international environment
• Team spirit and good communication skills.

CVs should be sent to Maria Nicolau at

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