Are you passionate about drug safety and literature monitoring? Clarivate, a global leader in information services, is seeking a talented Pharmacovigilance (PV) Specialist to join their dynamic team!
🏢 Company: Clarivate
📍 Location: Noida, Uttar Pradesh, India (Hybrid)
💼 Position: Pharmacovigilance Specialist/Lead PV Specialist
🎓 Education: Master’s Degree in Life Sciences, Health or Biomedical Sciences
⏰ Experience: Minimum 4 years in biomedical literature review and adverse event reporting
About Clarivate: We provide trusted insights and analytics to accelerate the pace of innovation. Our PV Literature team supports multiple customers across all therapeutic areas, offering a supportive working environment with opportunities to engage in different aspects of pharmacovigilance.
Key Responsibilities:
- 📊 Analyze biomedical literature for safety-relevant information
- 📝 Write concise narratives summarizing potential safety issues
- 🔍 Review and extract data from literature using specialized databases
- 🚀 Support creation of periodic safety update reports
- 💊 Monitor new drug and therapeutic categories for adverse effects
Ideal Candidate:
- 🧠 Strong knowledge of biomedical terminology and therapeutic areas
- 📚 Proficient in literature searches and data extraction
- ✍️ Excellent scientific writing and communication skills
- 🤝 Ability to work collaboratively in a team environment
- ⏱️ Strong time management and attention to detail
Bonus Qualifications:
- 🏅 Certification from a professional medical writer’s association
- 💻 Experience with commercial biomedical literature databases
- 🖋️ Scientific/medical writing background
Why Join Clarivate?
- 🌟 Be part of a global leader in information services and analytics
- 🌍 Work on projects with real-world impact on drug safety
- 📈 Opportunities for professional growth and development
- 🤝 Collaborate with experts across multiple therapeutic areas
How to Apply: “Apply Here”
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