Danielle Downer

Background

About Danielle Downer

Master’s-level Clinical Research Professional with 3 years of experience coordinating Phase I–IV clinical trials, with a strong foundation in regulatory documentation, protocol compliance, and patient-centered research operations. Currently supporting multi-sponsor ophthalmology studies with a focus on audit readiness, subject protections, and cross-functional coordination. Passionate about the intersection of science, ethics, and operational excellence in clinical research—and committed to continuous learning and professional development across both site and sponsor-facing environments. Open to collaboration, mentorship, and knowledge-sharing in clinical trial operations, compliance, and research integrity.