Senior PVASC Specialist III
Job ID: 434387
Function: Medical and Clinical – Pharmacovigilance
Location: Bengaluru, Karnataka, India
Site: Bengaluru Luxor North Tower
Employment Type: Full-Time
Experience Required: 5–9 years
Posted Date: 29 January 2026
Job Overview
GlaxoSmithKline (GSK) is seeking an experienced Senior PVASC Specialist III to join its global pharmacovigilance and safety organisation in Bengaluru. This role plays a critical part in ensuring patient safety by leading pharmacovigilance agreement (PVASC) compliance, safety case processing oversight, and quality assurance activities across global programs.
The position offers exposure to complex safety operations, cross-functional collaboration with global stakeholders, and opportunities to contribute to continuous improvement initiatives within a highly regulated, science-driven environment.
About GSK
GSK is a global biopharmaceutical company with a clear purpose: to unite science, technology, and talent to get ahead of disease together. With a strong focus on vaccines and specialty medicines, GSK aims to positively impact the health of 2.5 billion people by the end of this decade. The organisation fosters a culture that is ambitious for patients, accountable for impact, and grounded in integrity.
Key Responsibilities
Lead and monitor PVASC compliance for GSK and third-party partners, including routine HSI reconciliations and compliance checks.
Ensure adherence to global pharmacovigilance regulations and internal quality standards for adverse event reporting.
Perform quality assurance reviews of Individual Case Safety Reports (ICSRs) within global safety databases, identifying trends, risks, and compliance gaps.
Independently manage safety data maintenance across pharmacovigilance databases, EDMS platforms, PVASC websites, and shared repositories.
Collect, evaluate, analyse, and document safety information received from local operating company safety teams.
Generate and analyse standard safety listings and reports from pharmacovigilance databases.
Administer document storage, archiving, and inspection readiness activities in line with approved processes.
Support and participate in regulatory inspections and internal audits, including those involving licensing partners.
Contribute to the development, review, and maintenance of SOPs, guidance documents, and training materials.
Collaborate with internal stakeholders including SERMs, Business Development teams, operating companies, and external partners with minimal supervision.
Lead or contribute to process improvement initiatives related to systems, tools, and workflows, including EDMS enhancements.
Apply emerging technologies, including AI and data visualisation tools, to improve efficiency and quality in safety operations.
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, GVP, and clinical safety documentation.
Experience with pharmacovigilance databases and electronic case processing systems.
Proficiency in medical terminology and medical coding standards, including MedDRA.
Advanced computer skills with MS Word, Excel, PowerPoint, and SharePoint.
Experience using Power BI or other data visualisation tools.
Demonstrated ability to incorporate AI/ML technologies into daily operational workflows.
Strong organisational, analytical, and problem-solving skills with the ability to work independently under tight deadlines.
Proven stakeholder management skills with a collaborative, customer-focused approach.
What GSK Values
GSK values professionals who demonstrate integrity, clear communication, and a strong commitment to patient safety. The organisation encourages diverse perspectives and provides a supportive environment for continuous learning, career development, and meaningful global impact.
Inclusion & Accessibility
GSK is committed to an inclusive recruitment process and equal employment opportunity. Candidates requiring adjustments during the recruitment process are encouraged to contact the recruitment team for support.
Recruitment & Fraud Disclaimer
GSK does not charge any fees at any stage of the recruitment process and does not make unsolicited job offers. All official communications originate from verified GSK domains. Candidates are advised to remain vigilant against fraudulent recruitment activities.
SEO & Search Keywords
Senior PVASC Specialist jobs in Bengaluru, GSK Pharmacovigilance careers, Drug Safety Specialist India, PV Compliance roles, ICSR Quality Assurance jobs, Global Safety Operations careers, Medical and Clinical jobs India.
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