Stephen Carroll

Stephen Carroll

Site Director @ Celerion

About Stephen Carroll

Stephen Carroll is the Site Director at Celerion in Richmond, Virginia, where he has worked since 2009. He manages the daily operations of a research facility, overseeing participant recruitment and ensuring compliance with research guidelines.

Work at Celerion

Stephen Carroll has served as Site Director at Celerion since 2009. In this role, he manages the daily operations of a multi-discipline research facility located in Richmond, Virginia. His responsibilities include overseeing research plans, marketing strategies, and participant recruitment efforts. Carroll plays a crucial role in ensuring the recruitment, enrollment, and retention of over 20,000 study participants. He also provides consultation and coordination among various stakeholders, including study sponsors, research participants, and ancillary departments.

Education and Expertise

Stephen Carroll studied at Virginia Commonwealth University - School of Business, where he earned a Bachelor of Science degree in Business Management from 1993 to 1996. His educational background provides a strong foundation for his management and operational roles within the research facility. Carroll's expertise encompasses participant recruitment, compliance with research guidelines, and coordination among various stakeholders in clinical studies.

Background

Before joining Celerion, Stephen Carroll worked at MDS Pharma Services as a Participant Recruitment Manager from 2006 to 2009. His earlier experience includes an eight-year tenure at Circuit City Stores Inc. as Manager of Applicant Screening from 1996 to 2004. This diverse background in management and recruitment has equipped him with the skills necessary for his current role in overseeing research operations.

Achievements

In his role as Site Director at Celerion, Stephen Carroll has successfully overseen the recruitment and retention of a significant number of study participants, totaling over 20,000. He ensures compliance with client-mandated requirements and guidelines governing human subject research. His efforts contribute to the effective management of clinical studies and the overall success of the research facility.

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