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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.
Lead end-to-end supply chain planning for cell & gene therapies, coordinating manufacturing, viral vectors, and logistics to ensure reliable patient delivery and portfolio growth.
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…
Lead a team of CMC project managers at a biopharma company, overseeing drug development and commercialization from early phase through launch, aligning timelines with clinical and regulatory goals.
Lead market research and insights for HIV prevention products, analyzing healthcare provider and consumer data to guide commercial strategy at a biopharmaceutical company.
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.
Designs and leads a global trade compliance program ensuring adherence to international import/export laws across Gilead's pharmaceutical supply chain. Partners with Legal, Tax, and Finance on regulatory compliance, customs, risk management, and systems like SAP GTS.
Leads the strategy and delivery of advanced analytics, GenAI, and cloud-native platforms for clinical development at a biotech company, overseeing engineering teams and ensuring scalable, compliant solutions.
Oversee APAC supply chain for Gilead’s small-molecule and biologic drugs, leading demand planning, S&OP, and supply escalations to ensure product availability and minimize stockouts.
Lead a team developing biochemical, biophysical, and cellular assays to validate drug targets and advance therapies from discovery to clinical trials across small molecules, biologics, and novel modalities.
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…
Supervise a team of cell therapy manufacturing specialists in a cGMP biotech facility, ensuring compliance and production schedules while leading staff and troubleshooting processes.
Lead clinical pharmacology programs for inflammation therapies at a biopharma company, designing studies, analyzing data, and guiding drug development from early trials to regulatory submissions.
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