Brandon Jones

Brandon Jones

Brandon is skilled in preparing electronic regulatory submissions, medical writing, regulatory intelligence and contract administration.

Brandon has worked in the Pharmaceutical/Clinical Research field for the past 17years providing services for both Sponsors and CROs. 

Prior to pursuing a consulting career Brandon provided eCTD submission expertise (including IND, MAA, ANDA, SPL) and regulatory document production at CRO leader QuintilesIMS (now IQVIA).  He is skilled in eCTD submissions and communications with the FDA, Health Canada and other regulatory agencies worldwide.  Further, Brandon provided leadership and training for regulatory intelligence, medical writing, and managed the Corporate Standards Database for the Quality Assurance Compliance and Standards Department at Biogen Idec.  Previously, he was the Risk Management Coordinator at Ashfield Pharmacovigilance where he chaired the Safety Executive Committee (SEC) meetings, reported safety decisions, medical safety discussions and tracked Events of Interest (EOI).  He has served as a Contract Administrator, negotiating complex legal language and budgets, at QuintilesIMS (now IQVIA), PharmalinkFHI (now Novella), Inveresk Research and local law firms. 

Brandon has a degree in Business Administration and attended University of North Carolina at Chapel Hill for Journalism and Mass Communications.