Senior PVASC Specialist III
Location: Bengaluru, India (Luxor North Tower)
Job Type: Full-Time
Application Deadline: February 6, 2026
Job Requisition ID: 434387
About GSK
GSK is a global biopharma company with a clear purpose: to unite 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 this decade, GSK focuses on innovation in vaccines and specialty medicines across key therapeutic areas including respiratory, immunology, oncology, HIV, and infectious diseases. Our culture is rooted in integrity, accountability, inclusion, and a strong commitment to patient safety.
Position Summary
GSK is seeking an experienced Senior PVASC Specialist III to lead pharmacovigilance and safety case processing activities. This role plays a critical part in ensuring patient safety through accurate safety data handling, regulatory compliance, and quality oversight of adverse event reporting. The position involves close collaboration with cross-functional teams across India and global regions, offering high visibility, continuous learning, and career growth within a global drug safety organization.
Key Responsibilities
Lead and monitor compliance with Pharmacovigilance Agreements and Safety Committees (PVASC) for GSK and third-party partners, including routine HSI reconciliation and compliance checks.
Independently perform quality assurance reviews of adverse event reports within the global safety database, identifying, documenting, and escalating issues as required.
Maintain and manage pharmacovigilance databases, Electronic Data Management Systems (EDMS), PVASC web pages, and shared repositories.
Collect, evaluate, analyze, and document safety information received from local operating companies and partners.
Generate and manage standard safety listings and reports from safety databases.
Administer document storage, archival activities, and team sites in accordance with approved procedures.
Support external regulatory inspections and internal GSK audits of licensing partners under senior supervision.
Contribute to the development, maintenance, and revision of SOPs, guidance documents, and process documentation.
Collaborate with SERMs, Business Development teams, operating companies, and external stakeholders with minimal supervision.
Lead or contribute to process and system improvement initiatives, including EDMS enhancements.
Perform additional pharmacovigilance-related duties as assigned.
Required Qualifications & Experience
Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing, or a related health science discipline.
5 to 9 years of hands-on experience in pharmacovigilance or drug safety, including ICSR processing.
Strong working knowledge of global pharmacovigilance regulations, Good Pharmacovigilance Practices (GVP), and clinical safety documentation.
Proven experience with global safety databases and electronic case processing systems.
Sound understanding of medical terminology and medical coding standards such as MedDRA.
Proficiency in MS Word, Excel, PowerPoint, and SharePoint.
Experience with data visualization and reporting tools such as Power BI.
Ability to incorporate AI/ML tools into routine pharmacovigilance workflows.
Demonstrated ability to work independently, manage competing priorities, and meet tight regulatory timelines.
Strong analytical skills, sound judgment, and a results-driven mindset.
Excellent stakeholder management, communication, and cross-cultural collaboration skills.
What GSK Values
GSK values professionals who act with integrity, communicate clearly, and prioritize patient safety. We foster an inclusive environment that encourages diverse perspectives and supports continuous learning and professional development.
Inclusion & Accessibility
GSK is committed to inclusion and equal opportunity. Candidates requiring adjustments during the recruitment process are encouraged to contact the Recruitment Team at IN.recruitment-adjustments@gsk.com.
Important Notice
GSK does not charge any fee at any stage of the recruitment process and does not accept unsolicited agency referrals without prior written authorization. Candidates are advised to beware of fraudulent job advertisements or emails not originating from official gsk.com domains.
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