Fresher Pharmacovigilance Jobs | GSK PV Operations – ICSR Management

Pharmacovigilance Job Opportunity for Life Science Graduates | GSK PV Operations – ICSR Management | Bangalore Location

Apply for GSK’s Pharmacovigilance ICSR Management role in Bangalore. Suitable for Life Science graduates with fresh to experienced profiles. Last date: July 23, 2025.

Career in Pharmacovigilance with GSK – Bangalore Location

If you’re a Life Science graduate or experienced professional looking to build a future in Pharmacovigilance, GSK offers a dynamic full-time opportunity under its PV Operations – ICSR Management department at the Bengaluru Luxor North Tower facility. GSK, a global biopharma leader, is seeking candidates who are enthusiastic about safety data, global health impact, and regulatory compliance.

This opportunity is ideal for those aiming to gain end-to-end exposure in pharmacovigilance case handling, quality compliance, and global health data reporting.

The last date to apply is July 23, 2025.

About GSK: Driving Innovation in Biopharma

GSK (GlaxoSmithKline) is renowned for uniting science, technology, and talent to lead the healthcare space. With a strong focus on disease prevention, treatment innovations, and vaccine development, GSK operates in major therapeutic areas like infectious diseases, HIV, oncology, respiratory and immunology.

Their purpose-driven culture and investment in employee growth make it a preferred choice for healthcare professionals worldwide.

Key Responsibilities in ICSR Management

End-to-End Case Handling and Global Collaboration

• Handle the lifecycle of Individual Case Safety Reports (ICSR) from initial receipt to expedited regulatory submission.
• Collaborate with Safety Evaluation and Risk Management (SERM), local affiliates, and clinical operations to ensure compliance and timely reporting.
• Escalate potential issues to PV Operations Management and contribute to CAPA (Corrective and Preventive Actions).

Documentation and Audit Compliance

• Participate in inspection and audit readiness by maintaining detailed and accurate safety documentation.
• Upload, organize, and reconcile audit-related documents and regulatory filings.

Process Improvement and Technology Adaptation

• Develop and propose process optimization initiatives for global rollout.
• Support onboarding processes, training modules, and departmental IT functionalities.
• Use internal databases and collaborative platforms to streamline safety operations.

Required Education and Qualifications

• A degree in Life Sciences, Pharmacy, Biotechnology, or related healthcare disciplines.
• Freshers and professionals with up to 2 years of experience in pharmacovigilance, clinical research, or drug safety are encouraged to apply.

Call to Action

📩 Apply before July 23, 2025, to begin your journey in the life sciences domain with one of the most reputed global pharma organizations.

Apply directly on the official GSK job portal.

Or contact: askus@gsk.com for job-related verification and inquiries.

Summary Table for Google SEO Optimization