Join Clarivate as an Associate Content Editor – B. Pharma/ M. Pharma can Apply

Unlock Your Editorial Potential: Join Clarivate as an Associate Content Editor! Clarivate, a global leader in transformative intelligence, is seeking passionate individuals to join our dynamic team. As an Associate Content Editor, you’ll be part of a company that brings together enriched data, insights, analytics, and workflow solutions to empower knowledge, research, and innovation worldwide.

With deep domain expertise across various fields, Clarivate is committed to delivering trusted and transformative intelligence. Seize the opportunity to be a part of this exciting journey and make a meaningful impact in the world of content editing. Apply now and take the first step towards a rewarding career with Clarivate!

Job Title: Associate Content Editor

Department: Clinical Studies

Education: B. Pharm/M. Pharm/ M. Sc. in Biotechnology, Microbiology graduate

Experience:
1. Atleast 1 year of experience in analyzing and updating clinical reports.
2. In-depth knowledge of clinical trials, pharmaceutical drug pipelines, drug development and clinical phases.
3. Experience in secondary research related to clinical information

About the job
As an Associate/Content Editor in Clinical team, you will be responsible for actively seeking out information about Clinical Studies, analyze, cross reference, and update all new or previously updated information in the clinical records from various sources, which includes scientific meetings, conferences, trial registries, press releases and other possible internet sources.

We are looking for an Associate Content Editor /Content Editor to join our Clinical Studies team in Hyderabad. This is an amazing opportunity to work on Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. We have a great skill set in Clinical and we would love to speak with you if you have skills in Clinical/Drugs.

What will you be doing in this role?
1. Maintain Clarivate database with up-to-date and accurate Clinical trials information from a range of information sources
2. Accountable for the delivery of weekly targets
3. Ensure quality standards are observed
4. Ability to understand and interpret complex and detailed Trials & Drugs related information from source material
5. An inquisitive, analytical mind with strong problem-identification and solving skills

Hours of Work
45 hours in a week, working days Monday to Friday, working hours 9AM to 6PM IST, Hybrid working mode with 2-3 days a week.

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