GSK Hiring Literature Specialist (Pharmacovigilance) | Bangalore | Drug Safety Jobs

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Literature Specialist (Pharmacovigilance)

GSK
Bangalore
1–5 Years
Pharmacovigilance
Literature Review
Drug Safety
Full-Time

📄 About the Company

GSK is a global biopharmaceutical company focused on vaccines and specialty medicines, with a mission to positively impact 2.5 billion people by 2030.

GSK operates across key therapeutic areas including respiratory, oncology, HIV, immunology, and infectious diseases, combining science, technology, and innovation to get ahead of disease.

📌 Job Overview

GSK is hiring a Literature Specialist I in Bangalore to support global pharmacovigilance literature monitoring.

This role plays a critical part in drug safety, ICSR identification, signal detection, and regulatory compliance by reviewing scientific and medical literature.

🧪 Job Details – Literature Specialist I

Company: GSK

Job Title: Literature Specialist I

Location: Bengaluru, Karnataka

Experience: 1–5 Years

Employment Type: Full-Time

Application Deadline: 20 February 2026

🧾 Key Responsibilities

  • Perform pharmacovigilance literature surveillance as per global regulations
  • Screen and review scientific literature, abstracts, and citations
  • Identify ICSRs from published literature
  • Triage literature for signal detection and periodic safety reporting
  • Support Global Safety teams with accurate literature review outputs
  • Maintain up-to-date product knowledge and master drug lists
  • Conduct quality checks on literature screening activities
  • Collaborate with PV, medical affairs, and regulatory teams
  • Ensure timely and compliant delivery of literature monitoring outputs

🎓 Eligibility & Qualifications

  • B.Pharm / M.Pharm / Pharm.D
  • BSc / MSc – Life Sciences, Pharmacology, Medicine
  • 1–5 years experience in:
    • Scientific literature searching
    • Pharmacovigilance support
    • Medical or regulatory writing
    • Drug safety or clinical research (preferred)

🧠 Required Skills

  • Strong understanding of pharmacovigilance regulations
  • Excellent English communication & medical terminology skills
  • High attention to detail and analytical mindset
  • Experience with web-based literature databases
  • Ability to work in cross-functional global teams

💼 Salary & Benefits (Estimated)

  • 💰 ₹6,00,000 – ₹10,00,000 per annum
  • Competitive pharma industry compensation
  • Career growth in global drug safety operations
  • Inclusive, collaborative, and learning-driven culture
  • Exposure to global safety and regulatory programs
📌 Note Before You Apply:
We use a 15-second timer to encourage candidates to carefully read the job description before applying. Ensure your experience aligns with pharmacovigilance literature review requirements.

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