Teams at GSK

Lead end-to-end regulatory submissions to CDSCO/DCGI for pharmaceutical, biopharmaceutical, and vaccine clinical trials. Ensure compliance with Indian regulations (NDCT Rule, Drugs & Cosmetics Act), manage regulatory lifecycle in Veeva Vault, liaise with Global RA/Medical/Clinical/PV, evaluate regulatory intelligence, and maintain SOP and documentation standards.

Lead end-to-end regulatory submissions and lifecycle management for pharmaceutical, biologic and vaccine products in India. Manage CDSCO/SUGAM filings, clinical trial approvals, labeling/artwork, stakeholder coordination, Veeva Vault tracking, QMS compliance, and regulatory intelligence to support product approvals and lifecycle activities.

Lead planning and delivery of pharmaceutical products and brand strategies. Conduct market and competitor analysis (IMS/SMSRC), develop and execute marketing and in-clinic campaigns, manage budgets and P&L inputs, enable sales with training and materials, collaborate cross-functionally with commercial, medical, regulatory and supply teams, and measure performance using dashboards and forecasting tools to drive market share and sales growth.