Shannon Ruecker joined Biologics Consulting as an Electronic Publishing Specialist in May 2018.
Shannon comes to Biologics Consulting with over 3 years of regulatory submission experience. She previously worked for PAREXEL International as an Associate in the Regulatory Outsourcing Services group, assembling eCTD submissions primarily for the EU. In this role, she also gained experience assembling and validating eCTD submissions for Australia, New Zealand, Saudi Arabia, and Switzerland.
Prior to PAREXEL, Shannon worked for Arivis producing eCTD submissions in accordance with FDA requirements, and was the primary contributor to the publishing of original IND applications and master files. She is well-versed in eCTD guidance documents and was responsible for interpreting FDA and ICH specifications to produce business user requirements for the development of home-grown publishing software.
Shannon graduated summa cum laude from the University of California, Santa Cruz with a BA in Environmental Studies.
B.A. Environmental Studies, summa cum laude, University of California, Santa Cruz, CA (2010)