Department: Global Content Operations
Reports To: Content manager, China Pharmaceutical Industry
Clarivate™ is a global leader in providing trusted information and insights to accelerate the pace of innovation. We offer subscription and technology-based solutions coupled with deep domain expertise that cover the entire lifecycle of innovation – from foundational research and ideas to protection and commercialization.
Today, we’re setting a trail-blazing course to help customers turn bold ideas into life-changing inventions. Our portfolio consists of some of the world’s most trusted information brands, including the Web of Science™, Cortellis™, Derwent™, CompuMark™ and MarkMonitor™.
We employ 9,500 colleagues in more than 40 countries. Clarivate is a public company. We are listed on the New York Stock Exchange under the ticker NYSE:CCC.
Our life sciences knowledge and information are 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.
At Clarivate, we believe human ingenuity can transform the world and improve our future. That’s why we harness our global reach, curate our content, and invest in best-in-class technology and people.
Join the team that is improving the way the world creates, protects, and advances innovation.
Main Purpose of Role:
The Chinese Pharmaceutical content team is responsible for maintaining the timeliness and accuracy of investigational drug content on Cortellis Competitive Intelligence (CCI, https://www.cortellis.com/intelligence/) and other products within the Life Sciences portfolio. The Global Editorial Operations group gathers and analyses a variety of scientific and industry source data to provide value-add content for these databases, while the Business of Science team make efforts to provide comprehensive and timely data on Cortellis platform, including CCI, CRI (Cortellis Regulatory Intelligence), CTI (Cortellis Clinical Trial Intelligence) and CDI (Cortellis Deal Intelligence), etc.
The main role of the Content Specialist involves researching, identifying, translating, capturing and processing pharmaceutical content, specifically from China and Chinese language sources, updating it into Cortellis CI, and helping to maintain the quality of the database’s overall drug and company records. The sources for this information include regional conferences, which the role holder will be expected to attend, as well as direct engagement with relevant companies to gather source data. It is also expected that the Drug Information editor will take an active role in supporting development of drug, press release, company and associated clinical trials content and policy, and support of other Content Specialists in the Global Content Operations group in identifying data for their content sets.
Duties and responsibilities:
1. Identify, research and update pharmaceutical information into drug and company records in Cortellis CI and other products
2. Identify, research, translate and update press releases related to China pharmaceutical industry into Cortellis CI and the related workflow platform
3. Write and edit to a high standard for publication
4. Attend, report and update from national and international conferences as required
5. Other tasks cooperated with Global Editorial teams
6. Assist the manager in the development and maintenance of editorial policy, processes and procedures