Clarivate is seeking an Associate STEM Content Analyst (Clinical Studies) to join their Clinical Trials Intelligence team in Hyderabad. This is an excellent opportunity for professionals with a background in pharmaceuticals, biotechnology, or clinical research to contribute to Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence.
Key Responsibilities:
- Research, analyze, and update clinical trial records from various sources (clinical registries, conferences, press releases, etc.).
- Ensure accuracy and timeliness of clinical trial data in Clarivate databases.
- Meet weekly targets while maintaining high-quality standards.
- Interpret complex drug development and clinical trial phases information.
- Collaborate with a team of 20+ clinical research professionals.
Eligibility Criteria:
- Education: B.Pharma / M.Pharma / MSc in Biotechnology, Microbiology, or related fields.
- Experience: 0-1 year in clinical research, drug development, or pharmaceutical analysis.
- Skills Required:
- Strong understanding of clinical trials, drug pipelines, and phases of drug development.
- Excellent English communication (written & verbal).
- Ability to perform secondary research on clinical data.
Preferred Qualifications:
- Prior experience in secondary research related to clinical trials.
- Familiarity with clinical trial registries (ClinicalTrials.gov, WHO ICTRP, etc.).
Work Details:
- Working Days:Â Monday to Friday
- Shift: 9:00 AM – 6:00 PM IST
- Work Mode:Â Hybrid (Hyderabad-based)
About Clarivate
Clarivate is a global leader in providing analytics, insights, and scientific research solutions. Their Cortellis platform offers drug discovery and clinical trial intelligence, helping pharmaceutical companies accelerate innovation.
Why Join Clarivate?
✅ Work on cutting-edge clinical research data.
✅ Be part of a collaborative and skilled team.
✅ Hybrid work flexibility.
✅ Equal opportunity employer with a diverse work culture.
How to Apply?
