Pattie Skeens

Pattie Skeens has over 25 years of work experience in the pharmaceutical industry. Pattie has held various roles such as CQA Program Asset Lead at GSK, Director of Clinical Quality Assurance at Biopharmaceuticals, Associate Director of GCP/GLP Quality Assurance at TESARO, Inc., Head of GCP/GLP Quality Assurance at ImmunoGen, Inc., and Senior Manager of Clinical Trial Oversight and Compliance at Cubist Pharmaceuticals. Pattie also has experience at Millenium Pharmaceuticals and Pfizer, Inc., where they served as a Clinical Quality Lead. At Pfizer, they also held roles such as Clinical Statistical Programmer, Quality Assurance Auditor/IT Business Manager, Process Analyst, and Lead Validation Specialist.

Pattie Skeens obtained a Bachelor of Science degree in Computer Science from the University of New Haven/Charter Oak between 1996 and 2007. In 2012, they pursued a Master of Divinity degree in Hospital Chaplaincy at Andover-Newton Theological School, with their studies ongoing.