Associate STEM Content Analyst
🏢 About Clarivate
Clarivate is a global leader in research analytics and pharmaceutical intelligence solutions. Its Cortellis platforms support drug development, clinical trial tracking, and regulatory intelligence for pharmaceutical and biotech companies worldwide.
📌 Job Overview
Role: Associate STEM Content Analyst (Clinical Studies)
Location: Hyderabad (Hybrid)
Experience: Freshers / 0–6 months
Qualification: B.Pharm / M.Pharm / M.Sc (Biotech, Microbiology, Chemistry)
Work Hours: 9 AM – 6 PM
Employment Type: Full-Time
🔬 Role Summary
This role focuses on maintaining and analyzing global clinical trials intelligence data to support pharmaceutical R&D, regulatory strategy, and drug pipeline tracking.
If you want to strengthen your understanding of clinical data workflows, try this Clinical SAS Quiz to test your knowledge of clinical datasets and structures.
Professionals interested in safety reporting and drug development workflows can also explore this Drug Safety Analyst Quiz to strengthen their understanding of pharmacovigilance data.
🧾 Key Responsibilities
- Maintain and update clinical trials intelligence databases
- Analyze data from trial registries, conferences & pipeline sources
- Interpret drug development stages & clinical trial phases
- Cross-reference investigational & marketed drug data
- Ensure strict quality control and productivity targets
- Perform secondary research on clinical studies
- Track pharmaceutical pipeline intelligence
🎓 Required Qualifications
- B.Pharm / M.Pharm
- M.Sc Biotechnology, Microbiology, Chemistry
- Freshers welcome
- 0–6 months experience in clinical report analysis (optional)
🧠 Required Knowledge & Skills
- Understanding of clinical trials & drug development lifecycle
- Knowledge of clinical phases (Phase I–IV)
- Analytical & research interpretation skills
- Strong written & verbal communication
- Ability to interpret complex clinical study data
⭐ Preferred Skills
- Experience with secondary clinical research
- Familiarity with pharma databases
- Understanding of global regulatory frameworks
🌍 Why Join Clarivate?
- Exposure to global pharmaceutical R&D intelligence
- Hands-on experience with Cortellis platforms
- Hybrid work model & work-life balance
- Career pathways into regulatory intelligence & data science
- Stable corporate environment with growth opportunities
💰 Estimated Salary
₹3,00,000 – ₹4,50,000 per annum (Hyderabad IT-Pharma hybrid roles)
This role requires understanding of clinical trials and drug development processes. Reviewing clinical research fundamentals and pharmacovigilance data concepts can improve your selection chances.
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