Laura Jones
About Laura Jones
Laura Jones is the Director of Product Management at ArisGlobal, specializing in regulatory information management. She has over two decades of experience in regulatory affairs and system design, with a strong focus on electronic submissions and compliance.
Current Role at ArisGlobal
Laura Jones serves as the Director of Product Management for Regulatory Information Management (RIM) at ArisGlobal. She has held this position since 2022, contributing to the development and management of product strategies that align with regulatory requirements. Her role involves overseeing product lifecycle management and ensuring that the solutions meet the needs of clients in the pharmaceutical and biotechnology sectors.
Professional Experience in Regulatory Affairs
Laura Jones has extensive experience in regulatory affairs, having worked in various capacities across several organizations. She was the Associate Director of Regulatory Operations at ACADIA Pharmaceuticals from 2013 to 2017. Prior to that, she served as the Senior Manager of Regulatory Affairs Operations at Baxter Healthcare Corporation from 2001 to 2010. Her experience includes managing electronic submissions and submission management for global agency guidance and regulations.
Educational Background
Laura Jones studied at San Diego State University, where she earned a Bachelor of Science in Information Systems. Her studies spanned from 1995 to 2010, reflecting a commitment to her education over 15 years. Additionally, she attended Grossmont College, achieving an Associate of Science in Business Administration from 1993 to 1995.
Achievements in Electronic Submissions
Laura Jones has specialized in electronic submissions and submission management, participating in the FDA's Electronic Submissions Gateway (ESG) pilot test group. Her contributions to this initiative earned her a distinguished recognition award, highlighting her expertise in navigating complex regulatory environments.
Technical Proficiency and Compliance Expertise
Laura Jones is proficient in a range of R&D technologies, including CoreDossier, InSight Suite, ISI Publisher, and eCTD Xpress. She has extensive experience in validating quality systems to ensure compliance with 21 CFR 11 and the ISO 9600 series, demonstrating her commitment to maintaining high standards in regulatory processes.