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Oversee R&D quality audits, inspections, CAPA management, and regulatory compliance for cancer therapies in APAC, ensuring GxP standards and PMDA/NMPA alignment.
Oversee clinical trials for antiviral therapies, focusing on hepatitis, by designing protocols, monitoring safety, analyzing data, and ensuring regulatory compliance to bring new treatments to market.
Oversee early-phase clinical trials for antiviral therapies, managing budgets, timelines, and cross-functional teams to ensure regulatory compliance and high-quality data for drug development.
We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs…
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve…
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