Pamela Strode
About Pamela Strode
Pamela Strode serves as the Senior Vice President of Regulatory Affairs and Quality Assurance at Fulcrum Therapeutics, where she has worked since 2019. With over 35 years of experience in the pharmaceutical industry, she has held senior roles at several biotech companies and possesses a strong background in microbiology.
Work at Fulcrum
Pamela Strode has served as the Senior Vice President of Regulatory Affairs and Quality Assurance at Fulcrum Therapeutics since 2019. In this role, she has focused on regulatory strategies and quality assurance processes to support the company's mission in addressing unmet medical needs. Strode has been instrumental in modulating gene expression strategies, which are critical for the development of therapies for genetically defined diseases. Her leadership in regulatory affairs helps ensure compliance with industry standards and facilitates the advancement of Fulcrum's innovative treatments.
Previous Experience in Regulatory Affairs
Before joining Fulcrum Therapeutics, Pamela Strode held significant positions in regulatory affairs at several biotech companies. She worked as the Senior Vice President of Regulatory Affairs and Quality Assurance at Epizyme from 2016 to 2019. Prior to that, she served as Vice President of Regulatory Affairs at Cerulean Pharma, Inc. from 2014 to 2016. Strode's extensive experience in regulatory roles has contributed to her deep understanding of the pharmaceutical industry's regulatory landscape.
Career Background in the Pharmaceutical Industry
Pamela Strode has a career spanning over 35 years in the pharmaceutical industry, with a strong focus on regulatory affairs and quality assurance. Her career began at Bristol-Myers Squibb, where she worked as a Scientist and Manager in Regulatory Affairs from 1985 to 1994. She then spent 20 years at Boehringer Ingelheim as Executive Director of Regional Regulatory Affairs, further solidifying her expertise in the field. Strode's background includes a variety of roles that have equipped her with a comprehensive understanding of regulatory processes.
Education and Expertise
Pamela Strode holds a Bachelor of Science degree in Microbiology from Rutgers University, where she studied from 1977 to 1981. She also earned a Master's degree from Temple University between 2009 and 2013. Her educational background in microbiology supports her expertise in regulatory affairs, particularly in the context of genetically defined diseases. Strode's academic credentials, combined with her extensive industry experience, position her as a knowledgeable leader in regulatory affairs and quality assurance.