Danielle Murray

Danielle Murray is a Senior Director in Global Regulatory Affairs CMC Vaccines at Merck, where they manage activities as the CMC product lead for multiple post-approval global products. They are responsible for regulatory strategy development, submission preparation, and cross-functional collaboration to ensure product success. With over 11 years of experience in assay development, validation, and analytical troubleshooting for vaccine projects, Danielle has demonstrated expertise in GMP/GLP compliance and regulatory submissions. Currently pursuing a Bachelor of Science in Biology at Moravian College, they continue to enhance their knowledge and skills in the field.