Provide support to the BOM with SET related activities and participate in relevant cross functional meetings, as needed, throughout the life-cycle of a clinical trial Review biospecimen handling sections of ICF template; provide input and guidance to Clinical Operations (CLO) on any site, country or EC specific modifications to the ICF Entry of study-related data in the clinical biospecimen inventory tracking system for each supervisor-assigned study prior to First Patient In (FPI). Set-up and maintain all planned biospecimen-relevant information including details for each biospecimen collected. Maintain relevant documentation in clinical biospecimen inventory tracking system Perform continuous tracking of clinical trial collected biospecimens. Support BOM with biospecimen tracking and reconciliation activities for all assigned studies in BioMarin's in-house clinical biospecimen inventory tracking IT system. Fulfill analysis requests for use of samples Escalate queries that cannot be resolved within an agreeable timeframe to the BOM Address biospecimen related queries from Translational Sciences/Research Work with relevant parties to track biospecimen specific information to assist researchers with selecting of biospecimens for testing Participate in CBM functional process improvement projects, as needed

BA/BS in life sciences or related degree. Experience in lieu of education accepted. 2 years of relevant experience working in the pharmaceutical industry (including CROs, clinical sites, labs and biorepositories). 1 year of relevant technical experience working with biospecimen management, lab management, biobanking, or similar organizations.