Lisa Portale

SVP, Regulatory Affairs at Poseida Therapeutics

Ms. Portale is currently Senior Vice President, Regulatory Affairs, after joining Poseida in early 2019 as a vice president. She has more than 25 years of experience integrating regulatory strategy into drug development and precision medicine across multiple therapeutic areas. Her prior roles include serving as regulatory strategist and global portfolio lead for Pfizer and serving in several Regulatory Affairs roles of increasing responsibility at Phenomix Corporation, Neurocrine Biosciences, Medtronic, and Perrigo Company. Her experience spans oncology/immuno-oncology, cardiovascular, endocrinology, neuroscience, and combination products including the development of novel biological structures like ADCs, bi-specifics, CAR-Ts, nanoparticles, therapeutic/oncolytic vaccines, and traditional monoclonal antibodies. She received a B.S. in biology and biological sciences from Michigan State University and is RAC certified.

Timeline

  • SVP, Regulatory Affairs

    Current role

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