Cindy Everaert is an experienced professional in regulatory affairs and clinical operations, currently serving as a Regulatory Information Management System (RIMS) Specialist at ProductLife Group since August 2023. Previous roles include Regulatory Affairs Manager Key User for RIM Veeva Vault at Pierre Fabre Group and over 15 years at GSK, where responsibilities spanned from Regulatory Information Management Senior Administrator to various data management positions. Additional experience includes roles at Eli Lilly and Company, where duties involved clinical trial supply coordination and operations. Cindy's educational background includes a degree from Saint-Louis Bruxelles (1993-1997).