Liz Christiansen

Liz Christiansen has over 18 years of experience in the biopharmaceutical industry. Liz began their career in 2003 as Executive Administrator to VP Clinical Development/Regulatory Operations at Salmedix, Inc. In 2006, they joined Arena Pharmaceuticals as a Technical Writer II, where they were responsible for supporting the Pharmaceutical Development department for all technical writing and document control systems. In 2011, they moved to Ambit Biosciences as Document Control Manager, Regulatory Affairs, where they were responsible for formatting, preparing and publishing clinical and nonclinical study reports in preparation for submissions. In 2014, Liz started their own consulting business, Christiansen Consulting, as a Regulatory Affairs Consultant. In 2015, they joined Heron Therapeutics, Inc. as Manager, Regulatory Operations, where they managed regulatory submissions and information dossiers for clinical trials and registration. In 2017, Liz moved to Arena Pharmaceuticals, Inc. as Senior Manager Regulatory Affairs and then Manager Regulatory Affairs. Liz is currently employed as Director, Regulatory Operations, RIMS/DMS Lead at Denovo Biopharma.

Liz Christiansen obtained their undergraduate degree in Psychology and Speech Pathology from Southern Illinois University, Carbondale. In December 2022, they completed certification as a Vault Platform Associate Administrator and Vault Submissions Associate Administrator from Veeva Training Services.