Elaine Alambra

Elaine serves as the Vice President of Regulatory Affairs and Quality Assurance for Caribou Biosciences. She has more than 30 years of experience in regulatory affairs and quality assurance with biotechnology, pharmaceutical, and medical device companies in all phases of development in multiple therapeutic areas, including immunology (vaccines), oncology, ophthalmology and dermatology. Previously, Elaine was Executive Director of Regulatory Affairs at Dynavax Technologies during which time she lead the regulatory effort for HEPLISAV-B® and its US BLA approval and European licensing applications. Elaine has held a variety of regulatory and quality positions of increasing responsibility at Allergan, Santen Pharmaceuticals, PrisMedical, and Dey Laboratories. Elaine holds a B.S. in Biology from the University of California, Irvine.