Editorial analyst

Description de l'offre

Thomson Reuters is the world's leading source of intelligent information for businesses and professionals. We combine industry expertise with innovative technology to deliver critical information to leading decision makers in the financial, legal, tax and accounting, scientific, healthcare and media markets, powered by the world's most trusted news organization. Our scientific knowledge and information is essential for drug companies to discover new drugs and get them to market faster, for researchers to find relevant papers and know what's newly published in their subject, and for businesses to optimize their intellectual property and find competitive intelligence.

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 Thomson Reuters' 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.

Duties:

·  Research news releases and other information sources
·  Analysis of news alerts and researched articles on current pharmaceutical markets
·  Editing all copies to a high standard for publication
·  Update the Cortellis RI database
·  Undertake any other reasonable duties as requested by the line manager on a permanent or temporary basis

We are the leading source of intelligent information for the world's businesses and professionals, providing customers with competitive advantage. Intelligent information is a unique synthesis of human intelligence, industry expertise and innovative technology that provides decision-makers with the knowledge to act, enabling them to make better decisions faster. We deliver this must-have insight to the financial and risk, legal, tax and accounting, intellectual property and science and media markets, powered by the world's most trusted news organization.

About the IP & Science Business of Thomson Reuters
The IP & Science business is a global provider of information solutions to assist professionals at every stage of research and development and ensure they maintain and extract maximum value from their intellectual assets.

IP & Science is part of Thomson Reuters ( www.thomsonreuters.com), the world's leading source of intelligent information for businesses and professionals. Scientific information solutions can be found at thomsonreuters.com.

Profil recherché

Skills / Experience:

Essential:

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

·  Good command of any other European languages (e.g. Italian)
·  Editing and proofreading experience
·  Mastering the legislative process in France would be a plus
·  Background in life sciences
·  Understanding of the pharmaceutical/medical device industry and its key commercial drivers
Qualifications:

·  Communication/Editorial/Linguistic
At Thomson Reuters, we believe what we do matters. We are passionate about our work, inspired by the impact it has on our business and our customers. As a team, we believe in winning as one - collaborating to reach shared goals, and developing through challenging and meaningful experiences. With over 60,000 employees in more than 100 countries, we work flexibly across boundaries and realize innovations that help shape industries around the world. Making this happen is a dynamic, evolving process, and we count on each employee to be a catalyst in driving our performance - and their own.

As a global business, we rely on diversity of culture and thought to deliver on our goals. To ensure we can do that, we seek talented, qualified employees in all our operations around the world regardless of race, color, sex/gender, including pregnancy, gender identity and expression, national origin, religion, sexual orientation, disability, age, marital status, citizen status, veteran status, or any other protected classification under country or local law. Thomson Reuters is proud to be an Equal Employment Opportunity/Affirmative Action Employer providing a drug-free workplace.

Intrigued by a challenge as large and fascinating as the world itself? Come join us.

To learn more about what we offer, please visit careers.thomsonreuters.com.

More information about Thomson Reuters can be found on thomsonreuters.com.

Please note that as an internal applicant, to apply for this role you are obliged to notify your current manager. You will however be able to have an initial discussion with the recruitment manager about the role in complete confidence.