Senior Safety Evaluation Scientist III – Literature
Location: Bengaluru, Karnataka, India
Employment Type: Full Time
Function: Medical & Clinical | Pharmacovigilance
Industry: Biopharmaceuticals
Job ID: 434138
Posted Date: January 23, 2026
Work Site: Bengaluru – Luxor North Tower
About GSK
GSK is a global biopharmaceutical company committed to uniting science, technology, and talent to get ahead of disease together. With bold ambitions to positively impact the health of 2.5 billion people by the end of the decade, GSK focuses on discovering and delivering innovative vaccines and medicines across key therapeutic areas including respiratory, immunology, oncology, HIV, and infectious diseases.
Role Overview
The Senior Safety Evaluation Scientist III – Literature plays a critical role in pharmacovigilance and signal detection by performing comprehensive safety literature assessments in compliance with global regulatory requirements and GSK standards. This role supports aggregate safety reporting, signal management, and vendor oversight while ensuring robust, inspection-ready documentation and adherence to regulatory timelines.
The position requires strong expertise in safety literature review, post-marketing surveillance, and cross-functional collaboration within a global drug safety environment.
Key Responsibilities
Safety Literature & Signal Detection
Screen and review scientific literature, abstracts, and citations for inclusion in aggregate safety reports and identification of potential safety signals.
Maintain up-to-date product and therapeutic area knowledge to support accurate literature evaluation.
Support Safety Evaluation and Risk Management (SERM) product specialists with ad hoc literature searches and data collection.
Collaborate with SERM physicians and specialists to prioritize, review, escalate, and document safety findings and signal evaluations.
Pharmacovigilance Operations & Compliance
Ensure timely execution of safety literature activities in line with internal procedures, regulatory requirements, and defined timelines.
Maintain inspection-ready documentation and act as a point of contact during audits and regulatory inspections.
Identify operational issues and work proactively with cross-functional teams to resolve them efficiently.
Participate in continuous process improvement initiatives to strengthen pharmacovigilance and literature review processes.
Collaboration & Stakeholder Engagement
Maintain effective organizational networks across pharmacovigilance, medical, and clinical functions.
Demonstrate a service-oriented approach while working in a matrix, interdisciplinary environment.
Education & Experience Requirements
Educational Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing, or a related health science discipline (mandatory).
Experience Required
Minimum 7 years of experience in pharmacovigilance, drug safety, safety literature screening, medical affairs, or clinical research.
Prior experience within the pharmaceutical or biopharmaceutical industry is required.
Experience in post-marketing surveillance, signal detection, or regulatory safety activities is strongly preferred.
Technical & Professional Skills
Strong knowledge of post-marketing safety regulations and pharmacovigilance methodologies.
Understanding of causality assessment principles and safety signal evaluation.
Experience in scientific literature review, data gathering, synthesis, analysis, and interpretation.
Working knowledge of global pharmacovigilance regulations relevant to SERM activities.
Proficiency in medical and drug terminology with basic understanding of assigned therapeutic areas.
Excellent written and verbal English communication skills, particularly in scientific and medical contexts.
Ability to independently evaluate data, draw conclusions, and support evidence-based decision-making.
What GSK Values
GSK values professionals who prioritize patient safety, demonstrate integrity, and communicate with clarity and accountability. The organization fosters an inclusive, collaborative culture where diverse perspectives are encouraged, and continuous learning and professional development are actively supported.
Why Join GSK
Competitive base salary with annual performance-based bonus
Flexible working arrangements for eligible roles
Comprehensive healthcare and wellbeing programs
Strong learning, development, and career progression opportunities
Inclusive and purpose-driven global work environment
Inclusion & Equal Opportunity
GSK is an equal opportunity employer committed to inclusion and accessibility. Candidates requiring adjustments during the recruitment process are encouraged to reach out to the recruitment team.
Important Notice
GSK does not charge any fees at any stage of the recruitment process and does not accept unsolicited agency referrals without prior authorization. Candidates are advised to remain vigilant against fraudulent job advertisements.
Apply through thepharmadaily.com to explore global pharmacovigilance and drug safety career opportunities with GSK.
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