Moriah Wells

Background

About Moriah Wells

I'm a detail-driven research operations professional with 3+ years of experience supporting clinical trials, coordinating multi-site research projects, and driving process improvements in both nonprofit and industry settings. My expertise spans oncology trial administration, cross-functional project coordination, documentation management, and stakeholder engagement—from early-phase research through national program initiatives. In my current role at the National Organization for Rare Disorders (NORD), I support the Rare Disease Centers of Excellence by managing project workflows, facilitating team communication, and co-authoring patient and provider-facing resources published to expand access to telemedicine. Prior to this, I worked in the biotech industry, where I supported global clinical trials, tracked regulatory documents, maintained Trial Master Files (TMFs), and mentored new team members across international teams. I bring a unique blend of technical skill and mission-driven focus—equally comfortable analyzing timelines and deliverables as I am engaging with patient advocacy efforts. I thrive in fast-paced environments, ask the right questions, and take ownership of my work with a focus on quality, impact, and growth. Core Skills: Clinical Trial & Research Operations Project Coordination & Stakeholder Communication Document Control & Quality Assurance Healthcare Process Improvement Cross-Functional Collaboration Platforms: Veeva Vault, Medidata RAVE, Microsoft Office Suite, Google Workspace Actively open to high-impact opportunities in clinical research, healthcare project management, or operations leadership roles where I can make a measurable difference.