Sandra Overfield
About Sandra Overfield
Sandra Overfield is a Protocol Manager with experience at Bristol-Myers Squibb and i3 Innovus. She holds a Master’s Degree in Psychology from the University of Evansville.
Title
Sandra Overfield currently holds the position of Protocol Manager. In this role, she is responsible for overseeing protocol development, implementation, and compliance within clinical trials or similar undertakings. Her expertise ensures that projects adhere to regulatory requirements and meet set standards.
Work Experience at Bristol-Myers Squibb
Sandra Overfield has extensive experience at Bristol-Myers Squibb, Princeton, New Jersey. She served as Associate Director, CCO, and as a Protocol Manager. In these roles, her responsibilities likely included project leadership, clinical protocol development, and ensuring compliance with regulatory standards. Her long-term association with Bristol-Myers Squibb showcases her dedication and expertise in the pharmaceutical sector.
Role at i3 Innovus
Sandra Overfield worked as a Medical Monitor at i3 Innovus from 2009 to 2010. In this capacity, she would have been responsible for the safety and efficacy of clinical trials, ensuring that studies adhered to ethical standards and regulatory requirements. This role added to her robust experience in clinical research and protocol management.
Education and Expertise
Sandra Overfield completed her high school education at F. J. Reitz from 2099 to 2103. She then attended the University of Evansville, where she pursued and achieved a Master's Degree in Psychology. Her educational background in psychology provides a strong foundation for understanding human behavior, which can be vital in clinical trial management and protocol development.