GSK is seeking a Senior Literature Specialist III to support Global Safety literature screening activities for Individual Case Safety Reports (ICSRs) and signal detection in compliance with regulatory requirements. This role offers an excellent opportunity to grow your career in pharmacovigilance and drug safety while working with a leading global biopharma company.
Key Responsibilities
- Screen and review literature search results (articles, abstracts, citations) for ICSR identification.
- Triage literature for potential safety signals related to GSK-marketed and developmental products.
- Perform quality checks on articles reviewed by junior team members.
- Develop and optimize search strategies for literature surveillance.
- Collaborate with teams to resolve issues and improve processes.
- Support continuous process improvement initiatives in pharmacovigilance.
- Maintain expertise in PV regulations and scientific literature evaluation.
Why Join GSK?
GSK is a global leader in biopharmaceuticals, dedicated to uniting science, technology, and talent to get ahead of disease. We focus on vaccines, specialty medicines, and general pharmaceuticals, with core therapeutic areas including:
- Infectious Diseases
- HIV
- Respiratory & Immunology
- Oncology
Our Culture & Values
- Patient Focus – Putting patients first in all decisions.
- Transparency & Integrity – Maintaining ethical standards.
- Innovation & Performance – Driving scientific excellence.
- Inclusivity & Well-being – Ensuring a thriving workplace.
Eligibility Criteria
Basic Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or Pharmacology.
- Experience in pharmaceutical industry (drug safety, regulatory affairs, clinical development, or medical affairs preferred).
- Knowledge of pharmacovigilance regulations and methodologies.
- Strong English communication (written & verbal) with scientific/medical terminology.
- Proficiency in web-based applications and IT tools.
- Attention to detail and ability to work in a matrix environment.
Preferred Qualifications
- Master’s degree or higher in Health Sciences.
- Experience in literature screening for drug safety/signal detection.
- Strong analytical and problem-solving skills.
How to Apply
- Deadline: June 29, 2025
