Associate STEM Content Analyst (Clinical Studies)
Job ID: JREQ133654
Posted Date: September 11, 2025
Location: Hyderabad, Telangana, India
Division: Life Sciences & Healthcare
Work Mode: Hybrid
Work Hours: Monday to Friday, 9:00 AM – 6:00 PM IST
Employment Type: Full-Time
Summary
The Associate Content Editor will join Clarivate’s Clinical Studies team, working on Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. The role involves actively sourcing, analyzing, cross-referencing, and updating clinical study information from various sources to maintain an accurate and up-to-date database.
Key Responsibilities
Maintain Clarivate’s clinical trials database with current and accurate information from multiple sources, including scientific meetings, conferences, trial registries, press releases, and other online sources
Analyze and interpret complex clinical and drug-related information
Ensure delivery of weekly targets and maintain consistent quality standards
Identify issues and provide solutions with an inquisitive and analytical approach
Support the team in updating previously recorded information and integrating new data
Qualifications & Experience
Required
Bachelor’s or Master’s degree in Pharmacy (BPharm/MPharm), Biotechnology, or Microbiology
0–1 year of experience in analyzing and updating clinical reports
Knowledge of clinical trials, pharmaceutical drug pipelines, drug development, and clinical trial phases
Excellent written and verbal communication skills in English
Preferred / Desirable
Experience in secondary research related to clinical information
Strong analytical and problem-solving skills
About the Team
Clinical Studies team at Clarivate Hyderabad
Team size: ~20 members
Focus: Clinical and drug-related content for Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence
Work Environment & Culture
Hybrid work mode
Full-time, Monday to Friday
Equal employment opportunity employer, committed to diversity and inclusion
Compliance with all applicable non-discrimination laws and regulations
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