Yari Fontebasso

Senior Manager IT Compliance @Avidity Biosciences, Inc.

San Diego, CA, US
MOBILE NUMBERS
+13•••••••32

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WORK HISTORY

Sep 2025 — Present

Senior Manager IT Compliance @Avidity Biosciences, Inc.

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As Senior Manager of IT Compliance, I am architecting and leading Avidity\'s shift to a modern, risk-based compliance framework. My mission is to champion Computer Software Assurance (CSA), replacing documentation-heavy validation with streamlined, value-focused approaches that enable innovation.I partner with Quality, IT, InfoSec and other business teams to embed \'compliance-by-design\', integrating agile validation practices and automation to ensure our GxP systems meet global data integrity and regulatory standards without unnecessary overhead.

EDUCATION

2006 — 2011

University of Sussex

Doctor of Philosophy (PhD) , Biochemistry and Molecular Biology

2000 — 2005

Università degli Studi di Padova

Master of Science (MS) in Pharmaceutical Biotechnologies

1995 — 2000

Liceo Scientifico

High School Diploma, Science-based studies

SKILLS

Scientific WritingData AnalysisFunctional GenomicsDrug DiscoveryExperimental DesignHigh Throughput ComputingMolecular BiologyDna RepairBiochemistryNucleic Acid ExtractionCancer ResearchMolecular & Cellular BiologyFlow CytometryHigh Throughput Screening3d CulturesGeneticsMolecular and Cellular Biology TechniquesLife SciencesBiotechnologyShrna, Sirna, Transposon Mutagenesis, Crispr-Cas9Dna ElectrophoresisDrug DevelopmentYeast and Mammalian Cell CulturingCancerComputational AnalysisLaboratory RoboticsDrug Screening Setup and ValidationAssay DevelopmentLaboratory SkillsResearchRWestern BlottingHigh Throughput Data AnalysisCell BiologyTissue CultureRnaiLentivirus Production and Mediated DeliveryDnaPolymerase Chain Reaction (Pcr)Qpcr

ABOUT YARI FONTEBASSO

I am a multi-disciplinary leader with a 12+ year-long prior work as a research scientist. My experience includes computer systems validation activities, digital transformation initiatives, lab automation, creation and management of SQL databases and deployment of script-based analysis tools and computer systems that satisfy FDA 21-CFR Part 11 compliance guidelines in a GxP environment.Key core competencies- Laboratory asset management (R&D and GxP)- Expertise in digital solutions within highly regulated environments, bridging laboratory settings and IT- Developer of custom-built electronic solutions for compliant data analysis- Leader in computerized system validation and assurance, data integrity initiatives and digitization efforts in R&D to support GxP and non-GxP processes (including Electronic Lab Notebook, Registration and Sample Management, and Instrument Data Capture systems)- Effective bridge builder who understands and ensures alignment of scientific and laboratory requirements with enterprise technology strategies thanks to the prior extensive experience as a lab scientist.

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