STEM Content Analyst & Pharmacovigilance Roles
Clarivate
Hyderabad & Noida
Freshers Eligible
Hybrid Work
Clinical Research Analytics
Drug Safety
🏢 About Clarivate
Clarivate is a global leader in scientific intelligence, healthcare analytics, and life sciences data solutions. Its Cortellis platforms power pharmaceutical decision-making, clinical trial intelligence, and drug development strategies used by leading biopharma companies worldwide.
Working at Clarivate provides exposure to global drug pipelines, clinical trials, pharmacovigilance compliance, and real-world healthcare intelligence.
📌 Open Positions
- Associate STEM Content Analyst – Clinical Studies (Hyderabad)
- Associate Pharmacovigilance Specialist (Noida)
Work Mode: Hybrid | Monday–Friday
📊 Role 1: Associate STEM Content Analyst – Clinical Studies
- Maintain and update global clinical trials intelligence database
- Analyze trial registries, conferences, research publications & press releases
- Track drug pipelines and development phases
- Interpret complex clinical studies and pharmaceutical data
- Perform secondary research for clinical intelligence
- Ensure high data accuracy and productivity targets
Eligibility: B.Pharm, M.Pharm, MSc (Biotech/Microbiology)
Experience: Freshers – 6 months
💊 Role 2: Associate Pharmacovigilance Specialist
- Review biomedical literature for ICSRs & safety signals
- Identify adverse events and safety data
- Write safety narratives & summarize case data
- Monitor literature as per global PV regulations
- Maintain audit-ready drug safety documentation
- Ensure compliance with SOPs & global safety standards
Eligibility: Master’s in Pharmacy/Life Sciences/Biomedical Sciences
Experience: Fresher – 2 years
🎓 Required Skills
- Understanding of clinical trials & drug development phases
- Medical terminology & therapeutic area knowledge
- Strong analytical & research skills
- Scientific literature review & summarization
- Excellent written & verbal English
- Attention to detail & data accuracy
🌍 Why These Roles Are in High Demand
- Global drug pipeline expansion requires clinical intelligence
- Stricter pharmacovigilance regulations worldwide
- AI-driven healthcare analytics is rapidly growing
- Pharma companies depend on real-time safety & trial data
🚀 Career Growth Path
Clinical Intelligence Path:
- Analyst → Senior Analyst → Clinical Intelligence Specialist → Pharma Strategy Analyst
Pharmacovigilance Path:
- PV Associate → Drug Safety Associate → Signal Detection Specialist → Risk Management Scientist → PV Lead
💰 Salary Growth (India)
- Freshers: ₹3.5 – ₹6 LPA
- 2–4 Years: ₹7 – ₹12 LPA
- 5+ Years: ₹15+ LPA
- Global PV & Safety Roles: ₹30+ LPA
🧠 Skills to Learn to Get Selected
- Clinical trial phases & drug development lifecycle
- MedDRA & pharmacovigilance basics
- PubMed & scientific literature searching
- Drug pipeline & therapeutic area understanding
- Signal detection & safety evaluation basics
🎯 Who Should Apply?
- Pharmacy & life science freshers
- Candidates interested in clinical research & PV
- Those seeking non-lab pharma careers
- PV certification holders (advantage)
🌟 Why Join Clarivate?
- Exposure to global pharmaceutical intelligence platforms
- Hybrid work flexibility
- Strong foundation in drug safety & clinical analytics
- Career growth in research intelligence & PV
- Work with global biopharma clients
📌 Note Before You Apply:
Select the correct role before applying. Understanding responsibilities improves your chances of selection.
Select the correct role before applying. Understanding responsibilities improves your chances of selection.
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