Michele Bleiler has over three decades of experience in the pharmaceutical industry, currently serving as Associate Director of Regulatory Affairs International at Merck since 1989. Previously, Michele held positions such as Regulatory Writer, Manager of the Patient Informed Consent Specialist Group, and Patient Informed Consent Specialist within the same organization. Prior to joining Merck, Michele worked as a Toxicologist at Allentown General Hospital from 1987 to 1989. Michele's educational background includes a degree in College Prep with a focus on Science from Penn State University, attended from 1982 to 1986, and graduation from Emmaus High School in 1982.
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