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Serm Senior Scientist

0-2 years
Not Disclosed
10 Sept. 16, 2025
Job Description
Job Type: Full Time Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Description

Site Name: Bengaluru Luxor North Tower
Posted Date: September 15, 2025


Position Summary

Are you passionate about ensuring patient safety and advancing global health? As a Senior Scientist – Safety Evaluation and Risk Management (SERM), you will play a critical role in monitoring and evaluating the safety of GSK products. This role involves collaboration with cross-functional teams to identify, assess, and manage safety risks while ensuring compliance with global regulatory standards.

We seek candidates who are detail-oriented, proactive, and dedicated to making a meaningful impact on patient lives.


Key Responsibilities

  • Lead safety monitoring and evaluation for assigned GSK products.

  • Conduct signal detection and risk assessment activities.

  • Review and analyze Individual Case Safety Reports (ICSRs) and published literature to identify safety signals.

  • Draft and contribute to regulatory submissions, including periodic safety reports and risk management plans.

  • Collaborate with cross-functional teams to address safety-related queries and ensure compliance with regulatory standards.

  • Provide input into product labeling updates and other safety-related documentation.

  • Mentor and guide junior colleagues within the team.

  • Contribute to process improvement initiatives in safety operations.


Basic Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, or a related discipline.

  • Advanced degree preferred (Master’s, PhD, PharmD, or equivalent in Life Sciences/Medical field).

  • Experience in pharmacovigilance, safety surveillance, or drug development.

  • Familiarity with safety databases, tools, and global regulatory requirements.

  • Strong skills in safety data management, risk evaluation, and signal detection.

  • Proven ability to draft aggregate safety reports and risk management plans.

  • Excellent analytical, written, and verbal communication skills.

  • Ability to work effectively within a matrixed, global environment.


Why Join GSK?

At GSK, our purpose is to unite science, technology, and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by 2030 by developing innovative specialty medicines and vaccines across four therapeutic areas:

  • Respiratory, Immunology & Inflammation

  • Oncology

  • HIV

  • Infectious Diseases

We are committed to building an environment where people thrive, guided by our values of being ambitious for patients, accountable for impact, and doing the right thing.


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  • Any actions taken without authorization will not be recognized by GSK, and no fees will be paid.


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