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Jonathan Cascon has extensive work experience in the pharmaceutical industry. Jonathan is currently the Director of QA at Eidos Therapeutics, a position they have held since October 2020. Prior to this, they worked at BioMarin Pharmaceutical Inc. for nearly a decade, serving as the Associate Director of GVP Compliance in the Global Compliance & Ethics department. In this role, they were responsible for ensuring regulatory compliance in worldwide Drug Safety/Pharmacovigilance systems through audits, assessments, and training. Jonathan also contributed to the development and maintenance of the Pharmacovigilance System Master File (PSMF) and Risk Evaluation and Mitigation Strategy (REMS) documents.

Before joining BioMarin Pharmaceutical Inc., Jonathan worked at Genentech as a PV Compliance Quality Analyst from 2004 to 2011. In this position, they managed global case processing quality activities, compliance metrics, and supported PV inspections/audits. Jonathan collaborated with external business partners to address lateness issues in case exchanges and worked with team leaders to improve operational workflows.

Jonathan's earlier experience includes a role as a Drug Safety Coordinator at Actelion from 2003 to 2004. In this position, they performed data entry and coordinated the submission of expedited safety reports. Jonathan also worked as a Clinical Data Specialist at Sugen, Inc. from 1999 to 2003, providing support to management and staff, answering calls from the safety hotline, and sharing clinical trial information.

Overall, Jonathan Cascon has a strong background in pharmaceutical compliance, quality assurance, and drug safety operations.

Jonathan Cascon earned a Bachelor of Science (B.S.) degree in Business Administration from the University of San Francisco, where they studied from 1995 to 1999.