• Execute and coordinate decentralized, fully remote clinical research activities across autoimmune studies. • Own day-to‑day remote member operations—from recruitment and e‑consent to virtual follow‑up and remote data collection. • Ensure protocol adherence and high‑quality real‑world data. • Monitor protocol adherence and visit windows using remote tracking tools; document adverse events and concomitant medications based on member reports and records. • Maintain accurate and complete electronic study documentation, including source notes, case report forms, and digital regulatory binders. • Support IRB submissions, amendments, and continuing reviews with remotely managed documents, reports, and member‑facing materials. • Collaborate virtually with data, product, and operations teams to troubleshoot remote workflows and ensure data quality in decentralized studies.