Cindy Frommer

Cindy Frommer has extensive experience in the pharmaceutical industry. Most recently, they served as the Director of Clinical Operations at CorEvitas, LLC, where they were responsible for leading post-approval studies and registries. Their responsibilities included strategic planning, clinical study execution, and cross-functional team leadership. Cindy also oversaw patient recruitment and retention plans, data quality, and study costs.

Prior to their role at CorEvitas, Cindy held various positions at Merck and Schering-Plough Research Institute. At Merck, they served as an Associate Director of Clinical Research, focusing on emerging markets clinical development. Cindy also served as a Program Manager, leading projects in the respiratory, immunology, and cardiovascular areas.

During their time at the Schering-Plough Research Institute, Cindy worked as a Senior Clinical Project Manager, overseeing projects in immunology, hepatology, central nervous system, cardiovascular, and erectile dysfunction areas.

Overall, Cindy Frommer has extensive experience in clinical research, project management, and cross-functional team leadership in the pharmaceutical industry.

Cindy Frommer earned their Bachelor of Science degree from Montclair State University between 1993 and 1997.