Lilly Seidel
About Lilly Seidel
Lilly Seidel is a Trial Safety Scientist at Bristol Myers Squibb in Summit, New Jersey, with a background in pharmacy and extensive experience in safety surveillance and management.
Title
Lilly Seidel holds the position of Trial Safety Scientist at Bristol Myers Squibb. Her role is based in Summit, New Jersey, United States.
Current Role and Responsibilities
Lilly Seidel works as a Trial Safety Scientist at Bristol Myers Squibb. In this role, she supports the Lead Product Safety Physician in monitoring and managing the emerging safety profile of products. She leads logistics and coordination of Safety Management Team and Product Safety Review Meeting meetings. Additionally, Seidel drafts materials for Company Safety Committee meetings, conducts signal detection activities, and supports regulatory safety requests by obtaining data from clinical trials and global safety databases. She also helps determine the impact of safety issues on the product’s benefit/risk profile and provides input for safety publication strategies.
Previous Experience at Pfizer
Lilly Seidel previously worked at Pfizer, where she served as Associate Director from 2010 to 2019 in Peapack, New Jersey. Before that, she held the position of Safety Surveillance Specialist from 2004 to 2010 in Bridgewater, New Jersey. During her tenure at Pfizer, she gained substantial experience in safety surveillance and managing safety profiles of pharmaceutical products.
Experience at Medico Health Solution
Before her roles at Pfizer, Lilly Seidel worked at Medico Health Solution as a Registered Pharmacist from 1991 to 2004. This 13-year experience in Parsippany, New Jersey, allowed her to develop a strong foundation in pharmacy and healthcare.
Educational Background
Lilly Seidel studied Pharmacy at Saint John's University, where she earned a Bachelor of Science (BS) degree. Prior to that, she attended Nassau Community College and obtained an Associate of Science (AS) degree in General Biology. Her educational background has equipped her with a robust knowledge base essential for her roles in the pharmaceutical industry.