Pattie Skeens

Pattie Skeens has an extensive work experience in the pharmaceutical industry. Pattie started their career at Pfizer in 1994 as a Clinical Quality Lead and worked there until 2012. During their time at Pfizer, they also held roles as a Clinical Statistical Programmer, Quality Assurance Auditor/IT Business Manager, Process Analyst, and Lead Validation Specialist. Pattie then moved on to work at Millenium Pharmaceuticals as Quality Assurance from 2012 to 2013, and at Cubist Pharmaceuticals as Senior Manager, Clinical Trial Oversight and Compliance from 2013 to 2014. Pattie joined ImmunoGen, Inc. in 2014 and held positions as Associate Director, Registry and Late Phase Quality Assurance, and later as Head, GCP/GLP Quality Assurance until 2016. Pattie then worked at TESARO, Inc. as Associate Director, GCP/GLP Quality Assurance from 2017. In 2018, they joined Biopharmaceuticals as Director, Clinical Quality Assurance, and in 2019, they started working at GSK as CQA Program Asset Lead.

Pattie Skeens completed their Bachelor of Science degree in Computer Science from the University of New Haven/Charter Oak in 2007. Pattie then pursued further education by enrolling in Andover-Newton Theological School in 2012. Currently, their education history does not include any completion date for their Master of Divinity degree in Hospital Chaplaincy.