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Scott Vanderwerf

Principal Clinical Evidence Specialist @Medtronic

Portland, OR, US
EMAILS
[email protected]
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Nov 2022 — Present

Principal Clinical Evidence Specialist @Medtronic

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Portland, OR, US

EDUCATION

N/A

Oregon Health & Science University

Doctor of Philosophy (Ph.D.), Biochemistry and Molecular Biology

N/A

University of Portland

Technology Entrepreneurship Certificate Program

N/A

University of Washington

Bachelor of Science (B.S.), Biochemistry

SKILLS

Systems BiologyPharmacokineticsProteomicsNeurodegenerative DiseaseImmunoprecipitation3d PrintingStrategic PlanningCancer ResearchBiotechnologyProtein PurificationStart-UpsPre-Clinical StudiesMedical DevicesTechnology DevelopmentQrt-PcrRegulatory Strategy DevelopmentAssay DevelopmentIntellectual PropertyRegulatory SubmissionsGrant WritingDrug DevelopmentRare DiseasesEvent PlanningHplcRegulatory AffairsProtein ExpressionTechnology TransferFundraisingCell CultureBiocompatibilityDrug DiscoveryHigh Throughput ScreeningChromatographyCell BiologyProtein-Protein InteractionsMembrane TraffickingAnimal ModelsMolecular BiologyRegulatory ComplianceAddiction Research

ABOUT SCOTT VANDERWERF

Regulatory and clinical affairs director/consultant with broad medical device and pharmaceutical expertise, including U.S, Europe and China regulatory submissions, global regulatory and clinical strategy development, clinical study design and management, clinical data analysis and reporting, intellectual property asset development, and building strategic relationships.Diverse background in diabetes, cardiovascular disease, rare diseases, neurodegeneration, drug addiction, and digital health.

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