Clinical Data Standards professional supporting Data Management and Statistical Programming roles for over 22 years. As a CDISC specialist, I’ve demonstrated an understanding of clinical trial tools and processes, gaps in those processes, and created opportunities to make improvements for better CDISC harmonization and compliance across the enterprise. Core Competencies: CDISC/CDASH & SDTM Standards implementation, data integration, compliance tools, project management, mentor, coach and line management. Diversity and Inclusion advocate leading internal and industry initiatives to improve the clinical study inclusion of patients from marginalized populations. Proud LGBTQIA+ Ally. Disability Advancement Working Group lead team member, driving patient and communities' initiatives. Industry Participation: CDISC, PharmaSUG, PhUSE, DIA: Planning and Academic Committees & working groups. Currently an active member of CDISC: CAC Member, CDASH Co-Lead and SOGI working group member.