Clarivate is hiring an Associate STEM Content Analyst (Clinical Studies Team) in Hyderabad. This hybrid opportunity is ideal for B.Pharm, M.Pharm, and M.Sc (Biotechnology/Microbiology) graduates interested in clinical trials intelligence, drug pipeline analysis, and pharmaceutical research analytics.
The selected candidate will contribute to Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence, working closely with global clinical data sources. If you are looking to build a career in clinical research analytics, clinical trial database management, and drug development intelligence, this role offers strong industry exposure.
🔍 Key Responsibilities
As an Associate STEM Content Analyst, you will:
- Maintain and update Clarivate’s clinical trials database with accurate information
- Analyze and cross-reference clinical trial data from:
- Trial registries
- Scientific conferences
- Press releases
- Research publications
- Track pharmaceutical drug pipelines and clinical development phases
- Interpret complex clinical studies and drug-related information
- Deliver weekly productivity targets with high quality standards
- Perform secondary research related to clinical intelligence
- Ensure data accuracy in clinical trial intelligence platforms
This role requires strong analytical thinking, attention to detail, and the ability to interpret clinical trials and pharmaceutical drug development data.
🎓 Qualifications & Eligibility
Education Required:
- B.Pharm
- M.Pharm
- M.Sc (Biotechnology / Microbiology)
Experience:
- Freshers OR
- Up to 6 months of experience in clinical report analysis or clinical data updating
Required Skills:
- In-depth understanding of clinical trials and drug development phases
- Knowledge of pharmaceutical drug pipelines
- Strong written and verbal English communication skills
- Analytical mindset with problem-solving ability
Preferred:
- Experience in secondary research related to clinical information
🏢 Job Details
- Position: Associate STEM Content Analyst
- Department: Clinical Studies Team
- Work Mode: Hybrid (Monday–Friday)
- Location: Hyderabad, India
- Working Hours: 9:00 AM – 6:00 PM
- Experience Level: Freshers / Entry-Level
💼 Why Apply for This Clinical Trials Role?
- Exposure to global clinical trial intelligence databases
- Opportunity to work on pharmaceutical drug pipeline tracking
- Hybrid work model
- Entry into pharmaceutical analytics & research domain
- Strong foundation in drug discovery intelligence
For pharmacy and life sciences graduates, this role bridges clinical research, drug development, and pharmaceutical analytics, making it highly relevant for long-term career growth.
📩 How to Apply?
