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Luke Velders

Associate Director, Clinical Quality Assurance, Global Quality Assurance at GlaxoSmithKline

Luke Velders is a professional with a strong background in quality assurance in oncology and immunotherapy clinical trials, coupled with leadership and development skills. With a focus on the pharmaceutical industry, his aim is to lead and oversee quality and compliance activities. Luke's interests in medical ethics, quality assurance, pharmacovigilance, and health law align well with the rapidly evolving biopharmaceutical landscape. He aspires to establish robust frameworks to advance research and development, aiming for efficient FDA, MHRA, and EMA approvals in the US, UK, and EU, all while upholding ethical and regulatory standards.

Luke Velders
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Location

Greater Boston