Job Location: Hyderabad, Telangana, India
Clarivate(tm) is a global leader in providing solutions to accelerate the lifecycle of innovation. Our bold mission is to help customers solve some of the world’s most complex problems by providing actionable information and insights that reduce the time from new ideas to life-changing inventions in the areas of science and intellectual property. We help customers discover, protect and commercialize their inventions using our trusted subscription and technology-based solutions coupled with deep domain expertise.
We now have more than 8,500 colleagues in over 40 countries worldwide, and we work with over 200 partners to deliver value and success for our customers. Today, Clarivate is a publicly traded company, listed on the New York Stock Exchange under the ticker NYSE:CLVT.
Clarivate is committed to building, nurturing, and developing a diverse culture of belonging where new colleagues can bring their authentic self to work every day! Join us!
Associate Content Analyst/Content Analyst
As an Associate Content Analyst/Content Analyst, you will be responsible for the thorough, timely, and accurate interpretation of data relevant to biological drugs in the form of research, analysis, and delivery of weekly database filling milestones and also be responsible for improving the quality of the product. You would be part of a global team leveraging their diversity and local expertise to add value to the product.
We are looking for an Associate Content Analyst/Content Analyst to join our Biologicals Team in Hyderabad. This is an amazing opportunity to work. The team consists of 11 and is reporting to Team Manager. We have a great skill set in Drugs- Biologics and we would love to speak with you if you have skills in Drugs-Biologics.
About You – Experience, Education, Skills, And Accomplishments
- Work experience (A minimum of one year of experience as an Associate Content Analyst or Fresher)
- Knowledge and proven experience in secondary research involving biological drug-based patents, references, and conferences)
- Education (Masters in life science (Biochemistry, Immunology, Molecular Biology and Biotechnology), B. Tech/M. Tech (Biotech))
It would be great if you also had . . .
- Experience in secondary research related to biological drug-based patents, references, and conferences
What will you be doing in this role?
- To analyze the biological drug-based patents and references (articles/meeting abstract/clinical trial) and must understand the novelty clearly
- To identify one or more efficient biological drug/s and be able to describe them in a structured way
- Able to summarize the claim, novelty, and experiments described in the patent without grammatical and conceptual errors
- To do a comprehensive search for finding biological drug-related patents and references online
- Should meet weekly production volume and quality targets consistently; achieve KPI metrics
- Actively participate with the team and work towards process improvement
- Collaborate with ROW & Cross BU groups on demand
- To be flexible and adaptable toward process change
- To complete the tasks demanded by your line manager/director on a permanent or temporary basis
About The Team
The team works for the product CDDI. The team size is 11. The team includes Principal content analyst, Associate content analysts, content analysts, and senior Content analyst
Hours of Work
This is a full-time position
It is the policy of Clarivate to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, pregnancy, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Clarivate will provide reasonable accommodations for qualified individuals with disabilities.
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