GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.
Post : SERM Senior Scientist
Job Description
Position Summary : As a Senior Scientist in Safety Evaluation and Risk Management (SERM), you will play a key role in monitoring and evaluating the safety of our products. You will collaborate with cross-functional teams to identify, assess, and manage safety risks, ensuring compliance with global regulatory standards. We value candidates who are detail-oriented, proactive, and committed to making a positive impact on patient lives.
Responsibilities :
• Responsible for safety monitoring and evaluation of assigned GSK products.
• Conduct safety monitoring and evaluation for assigned products, including signal detection and risk assessment.
• Review and analyze individual case safety reports (ICSRs) and literature for safety signals.
• Draft and contribute to regulatory documents, including periodic safety reports and risk management plans.
• Collaborate with cross-functional teams to address safety-related queries and ensure compliance with regulatory requirements.
• Provide input on labeling updates and safety-related documentation.
• Mentor junior colleagues and contribute to process improvement initiatives within the safety team.
Candidate Profile
• Bachelor’s degree in Life Sciences, Pharmacy, or a related field. Advanced degree (e.g., Master’s, PhD, PharmD) in Life Sciences or a medical field preferred.
• Familiarity with safety databases and tools.
• Experience in pharmacovigilance, safety surveillance, or drug development.
• Knowledge of global regulatory requirements and safety data management.
• Strong analytical and communication skills.
• Ability to work effectively in a matrix environment.
• Experience in drafting aggregate safety documents and risk management plans.
Additional Information
Qualification : Bachelor’s degree in Life Sciences, Pharmacy
Location : Bengaluru Luxor North Tower
Industry Type : Pharma/ Healthcare/ Clinical research
Req ID : 427519
End Date : 15th October 2025
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