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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.
· 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
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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.