Priti Prasad, PhD, Ms
About Priti Prasad, PhD, Ms
Priti Prasad, PhD, Ms, is a Senior Manager in Regulatory Affairs specializing in Oncology at Sirnaomics, Inc. She has extensive experience in regulatory submissions and has worked with various organizations in the life sciences sector.
Current Role at Sirnaomics
Priti Prasad serves as the Senior Manager of Regulatory Affairs in Oncology at Sirnaomics, Inc. since 2021. In this role, she leads projects and contributes to various regulatory activities. Her responsibilities include the authorship of submissions such as pre-IND Type B Meeting Briefing information and Orphan drug Annual Reports. Prasad also provides scientific and regulatory guidance for marketing and promotional materials submitted to international regulatory authorities.
Previous Experience in Regulatory Affairs
Before joining Sirnaomics, Prasad held several positions in regulatory affairs. She worked as a Manager of Regulatory Affairs at Prolacta Bioscience from 2019 to 2021. Prior to that, she served as a Senior Associate in Regulatory Affairs at Amgen from 2017 to 2019. Her career also includes roles at GlaxoSmithKline as a Regulatory Specialist and at Pfizer Inc. as a Scientist in Medical Affairs & Safety, contributing to her extensive experience in the field.
Educational Background
Priti Prasad has a strong educational background in the sciences. She earned her Doctor of Philosophy (PhD) in Molecular Toxicology from the University of California, Los Angeles, completing her studies from 2010 to 2017. She also holds a Master of Science (MS) in Toxicology from Jamia Hamdard, obtained between 1996 and 1998, and a Bachelor of Science (BS) in Zoology from Delhi University, completed from 1993 to 1996. Her foundational education includes a high school diploma from Modern School, where she studied science from 1985 to 1993.
Teaching and Academic Contributions
Priti Prasad has contributed to academia through her role as a part-time faculty member at California State University, Northridge during the Spring semester of 2014. Additionally, she served as a Teaching Assistant in the UCLA Life Sciences Department from 2013 to 2015, assisting in various courses over three academic quarters. These experiences reflect her commitment to education and mentorship in the field of life sciences.
Regulatory Expertise and Contributions
Prasad has developed expertise in preparing regulatory dossiers in eCTD format for submissions to global regulatory authorities. She actively contributes to preclinical and clinical projects related to regulatory submission requirements by the US FDA. Her role involves supporting clinical trial submissions via IND for novel products across multiple indications, requiring collaboration with cross-functional teams to ensure compliance and successful outcomes.