Tara Oneill
About Tara Oneill
Tara Oneill is a Clinical Data Processing Specialist with extensive experience in clinical trials and data management. She has worked at Canfield Scientific since 2015 and previously held various roles at Town Sports International.
Current Role at Canfield Scientific
Tara Oneill serves as a Clinical Data Processing Specialist at Canfield Scientific, a position she has held since 2015. In this role, she provides photographic training and ongoing technical support to study site personnel across multiple clinical trials. Her responsibilities also include managing large-scale electronic image transfers to clients, ensuring the efficient handling of critical data.
Previous Experience at Town Sports International
Tara Oneill worked at Town Sports International for nine years, from 2002 to 2011. During her tenure, she held several positions, including Camp Manager/Art Director, Coordinator, and Assistant Kids Program Manager. These roles involved overseeing various programs and managing creative aspects of camp activities, contributing to the overall success of the organization.
Career Progression at Canfield Scientific
Before her current position, Tara Oneill was a Clinical Project Associate at Canfield Scientific from 2011 to 2015. In this capacity, she gained valuable experience in clinical data management and project coordination. Her transition from Clinical Project Associate to Clinical Data Processing Specialist reflects her growth and expertise in the field.
Education and Training Background
Tara Oneill studied at St. Thomas Aquinas College, where she acquired foundational knowledge that supports her current role in clinical data processing. Her educational background complements her professional experience, enabling her to effectively contribute to clinical trials and data management.
Contributions to Clinical Trials
In her current role, Tara Oneill assists Clinical Services Project Management Teams with projects that involve quality checking image data sets for FDA submission. This critical function ensures that the data submitted meets regulatory standards, playing a vital role in the success of clinical trials.