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Ethel Holtzclaw has extensive work experience in the field of regulatory affairs. Ethel'smost recent position was as the Associate Director of Global Regulatory Sciences - Informatics & Intelligence at Blueprint Medicines, where they started in July 2021. Prior to this role, they held the position of Senior Manager of Global Regulatory Sciences - Informatics from January 2020 to June 2021. Ethel also previously worked at Blueprint Medicines as a Regulatory Systems Consultant from July 2019 to January 2020.

Before joining Blueprint Medicines, Ethel worked at Shire as a Manager of Product License Support from January 2017 to January 2019. Prior to this, they held the position of Senior Specialist of Product License Support from May 2015 to December 2016.

Ethel also gained experience at Genpact as a Regulatory Affairs Manager from January 2014 to May 2015. Ethel started their career as a Senior Regulatory Affairs Associate at Genpact from December 2011 to December 2013.

In addition, Ethel worked at G&W Laboratories as a Regulatory Affairs Associate from May 2011 to November 2011.

Overall, Ethel Holtzclaw has a diverse background in regulatory affairs, with experience in various roles and responsibilities across different companies.

Ethel Holtzclaw earned a Bachelor's Degree in Biology/Biological Sciences from New Jersey City University in 2008. In 2015, they obtained a Master's Degree in Clinical Trial Sciences, specializing in Regulatory Affairs, from Rutgers University - Newark.