Christine Purcell
About Christine Purcell
Christine Purcell serves as a Regulatory Administrator at Yale University School of Medicine's Yale Cancer Center, bringing over a decade of experience in regulatory administration and clinical trial management. Her career includes roles at Pfizer, Bayer, and Envision Pharma, highlighting her expertise in compliance and research protocols.
Regulatory Administrator at Yale University
Christine Purcell serves as a Regulatory Administrator at Yale University School of Medicine, specifically within the Yale Cancer Center. She has held this position since 2010, accumulating over 14 years of experience in regulatory administration. Her role involves ensuring compliance with research protocols and managing regulatory processes within a leading cancer research institution.
Professional Experience at Pfizer Inc.
Christine Purcell worked at Pfizer Inc. in various capacities. She was a Project Administrator/Account Manager at Aquent from 2003 to 2005, where she contributed for two years. Additionally, she served as a Logistic Coordinator at Pfizer for six months in 2008. Her experiences at Pfizer provided her with insights into project management and logistical operations in the pharmaceutical industry.
Clinical Trial Coordination at Bayer
Purcell has experience in clinical trial management, having worked as a Clinical Trial Coordinator at Bayer from 2005 to 2007 for two years. This role involved overseeing various aspects of clinical trials, which enhanced her understanding of compliance and research protocols essential in the regulatory landscape.
Educational Background in Business Administration
Christine Purcell studied at Middlesex Community College, where she achieved a degree in Business Administration. This educational background has provided her with foundational knowledge in business principles, which supports her roles in regulatory administration and project management.
Versatile Skill Set in Clinical Research and Project Management
Christine Purcell possesses a versatile skill set that bridges clinical research and project management. She actively seeks roles that integrate these domains, reflecting her extensive experience in regulatory administration and clinical trial management. Her expertise indicates a strong understanding of compliance and research protocols.