Lauren Wiliams
About Lauren Wiliams
Lauren Williams is a Clinical Study Manager at Celerion, where she has worked since 2012. She oversees a team of clinical conduct associates and manages various aspects of clinical trial operations.
Work at Celerion
Lauren Wiliams has been employed at Celerion since 2005, holding two key positions: Regulatory Affairs Coordinator and Clinical Study Manager. As a Regulatory Affairs Coordinator, she has accumulated 19 years of experience, while her role as Clinical Study Manager has spanned 12 years since 2012. In these roles, she organizes and manages various meetings, including weekly teleconferences and site initiation meetings, and oversees a team of approximately 100 clinical conduct associates and agency nurses.
Education and Expertise
Lauren Wiliams earned a Bachelor of Science (B.S.) degree in Biology from Monmouth University, where she studied from 2000 to 2004. Her educational background provides a solid foundation for her work in clinical research and regulatory affairs. She also completed her high school education at Saint John Vianney High School, where she received her diploma in 2000.
Clinical Trial Management Skills
In her role as Clinical Study Manager, Lauren utilizes various databases and tools for effective clinical trial management. She is proficient in using Clinquick, Quicklooks, Sharepoint, and various portals and FTP sites. Her responsibilities include assisting with the dosing of healthy subjects with trial-related investigational products and managing the logistics of Phase 1 and early clinical research studies.
Audit Management
Lauren Wiliams plays a critical role in audit management at Celerion. She is responsible for closing out internal and external audits efficiently and assists with audits conducted by the FDA and other governing bodies. Her attention to detail and organizational skills contribute to the compliance and integrity of clinical trials.