Clarivate is seeking an Associate STEM Content Analyst to join the Experimental Pharmacology & Models team in Chennai. This role is an excellent opportunity for M.Pharm/B.Pharm graduates with 0-2 years of experience in pharmacology content analysis. You will work on Cortellis Drug Discovery Intelligence (CDDI), a leading platform that integrates biological, chemical, and pharmacological data for drug development research.
Key Responsibilities:
✔ Review, analyze, and update pharmacological activities in the internal database (CMS).
✔ Extract and update in vitro, in vivo, and ex vivo study data from patents, journals, conferences, and posters.
✔ Document pharmacological parameters, units, materials, and methods used in drug studies.
✔ Record drug details, including animal models, dosage, endpoints, and duration.
✔ Meet production volume and quality targets while maintaining accuracy.
✔ Stay updated on industry developments and contribute to process improvements.
✔ Ensure data consistency, quality, and compliance with guidelines.
✔ Follow safety protocols and support team objectives.
Qualifications & Skills:
- M.Pharm / B.Pharm degree.
- 0-2 years of experience in pharmacology content analysis & editing.
- Strong research and analytical skills.
- Attention to detail and ability to work in a fast-paced environment.
- Knowledge of drug discovery, experimental models, and pharmacological data.
About Clarivate
Clarivate is a global leader in scientific and academic research, patent analytics, and pharmaceutical intelligence. The Cortellis Drug Discovery Intelligence (CDDI) platform provides manually curated, validated R&D data used by scientists worldwide.
About the Team
The Experimental Pharmacology & Models team analyzes journals, patents, and meeting abstracts to provide critical drug discovery data. The team supports researchers studying disease models and therapeutic treatments.
Work Details
- Full-time position (40 hours/week).
- Shift: 9:00 AM – 6:00 PM IST.
- Hybrid work model (Chennai-based).