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 reviewΒ literature search resultsΒ (articles, abstracts, citations) for ICSR identification.
- Triage literature for potential safety signals related toΒ GSK-marketed and developmental products.
- PerformΒ quality checksΒ on articles reviewed by junior team members.
- Develop and optimizeΒ search strategiesΒ for literature surveillance.
- Collaborate with teams to resolve issues and improve processes.
- SupportΒ continuous process improvementΒ initiatives in pharmacovigilance.
- Maintain expertise inΒ PV regulationsΒ 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 FocusΒ β Putting patients first in all decisions.
- Transparency & IntegrityΒ β Maintaining ethical standards.
- Innovation & PerformanceΒ β Driving scientific excellence.
- Inclusivity & Well-beingΒ β Ensuring a thriving workplace.
Eligibility Criteria
Basic Qualifications
- Bachelorβs degreeΒ in Life Sciences, Pharmacy, Medicine, or Pharmacology.
- Experience inΒ pharmaceutical industryΒ (drug safety, regulatory affairs, clinical development, or medical affairs preferred).
- Knowledge ofΒ pharmacovigilance regulationsΒ and methodologies.
- StrongΒ English communicationΒ (written & verbal) with scientific/medical terminology.
- Proficiency inΒ web-based applicationsΒ and IT tools.
- Attention to detailΒ and ability to work in aΒ matrix environment.
Preferred Qualifications
- Masterβs degree or higherΒ in Health Sciences.
- Experience inΒ literature screening for drug safety/signal detection.
- StrongΒ analytical and problem-solvingΒ skills.
How to Apply
- Deadline:Β June 29, 2025
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