Literature Specialist

Roles & Responsibilities:
• Support global safety literature screening for ICSR identification and signal detection
• Perform pharmacovigilance literature surveillance as per regulatory requirements
• Screen and review literature (articles, abstracts, citations) for safety information
• Triage literature for GSK marketed and development products using defined criteria
• Support periodic reporting and signal detection activities
• Maintain up-to-date product knowledge and master drug lists
• Perform quality checks on triaged literature and ensure documentation accuracy
• Collaborate with PV, Medical Affairs, and Regulatory teams

Qualification:
• Bachelor’s degree in Life Sciences / Pharmacy / Pharmacology / Medical discipline

Experience:
• 1–5 years of experience in literature review, pharmacovigilance support, or medical writing
• Pharmaceutical industry experience preferred (Drug Safety / Regulatory / Clinical / Medical Affairs)

Skills:
• Working knowledge of pharmacovigilance regulations and methodologies
• Strong scientific literature searching and screening skills
• Good understanding of medical and scientific terminology
• Excellent attention to detail and analytical skills
• Strong communication, interpersonal, and teamwork skills
• Good computer skills and experience with web-based applications

About the Organization:
GSK is a global biopharmaceutical company focused on vaccines and specialty medicines, uniting science, technology, and talent to get ahead of disease together while prioritizing patient safety and public health.