Roles & Responsibilities:
• Screen and review literature search results (articles, abstracts, citations) for aggregate report inclusion and safety signal detection.
• Maintain up-to-date product knowledge to aid literature evaluation.
• Support SERM product specialists with ad hoc literature searches.
• Ensure timely discussions, escalations, and documentation of safety findings and signal review outcomes.
• Identify potential issues and interact with team members to resolve them.
• Participate in continuous process improvement initiatives.
• Maintain good documentation practice and serve as Point of Contact during inspections/audits.
• Build and maintain effective organizational networks.
Qualification:
• Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing, or related health science.
Experience:
• Minimum 7 years’ experience in pharmacovigilance, drug safety, literature screening, medical affairs, or clinical research.
• Pharmaceutical industry experience preferred, including drug safety, regulatory, clinical development, or medical affairs.
• Knowledge of post-marketing regulations and causality assessment principles.
Skills:
• Strong scientific literature review, data gathering, synthesis, and interpretation skills.
• Knowledge of key pharmacovigilance regulations and methodologies.
• Excellent written and verbal English communication skills, particularly in scientific/medical terminology.
• Ability to evaluate data and draw independent conclusions.
• Service-oriented attitude and effective teamwork in a matrix environment.
About the Organisation:
GSK is a global biopharmaceutical company focused on uniting science, technology, and talent to improve the health of 2.5 billion people by the end of the decade. GSK delivers innovative medicines and vaccines across respiratory, oncology, immunology, HIV, and infectious diseases while fostering a culture of inclusion, patient-centricity, and employee development.
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