Supported by a distinguished network of industry veterans, Phoenovix combines deep scientific expertise with strategic insights to help you navigate complex development, safety, and regulatory challenges with confidence.
Advisor – Pharmacovigilance & Drug Safety
With over 30 years of experience spanning clinical practice, academia, & the pharmaceutical industry including Novartis & AstraZeneca.
He was instrumental in establishing & expanding the Novartis Patient Safety Hub in Hyderabad, India into a major global safety organization, managing over 85% of the company’s worldwide safety activities. As Global Safety Program Lead at AstraZeneca, Sibin spearheaded the medical safety strategy for the blockbuster lung cancer therapy during a period of breakthrough FDA designations & global expansion. His experience includes oversight of established & development-stage products across multiple therapeutic areas, including oncology & cardio-renal-metabolic diseases, bringing a unique lifecycle perspective to drug safety & risk management.
Advisor – Regulatory & Medical Writing
Nomita Saxena is a pharmaceutical leader with over 20 years of experience in regulatory writing, clinical development, & global regulatory submissions at various organizations including AstraZeneca, Novo Nordisk, GSK, & Accenture.
Formerly a Senior Director at AstraZeneca, she led the establishment & growth of a Regulatory Writing Global Capability Centre, building high-performing teams & strengthening global delivery capabilities. Her career also includes leadership & medical writing roles at Novo Nordisk, GSK, & Accenture, where she contributed to clinical development, scientific communications, & regulatory documentation across multiple therapeutic areas & major regulatory authorities including US FDA, EMA & PMDA. As an independent consultant & advisor, she supports organizations in advancing writing excellence, operational effectiveness, AI-enabled innovation, & talent development.
Bengaluru, Karnataka, India
