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.

Bachelor’s degree in a related field (life sciences, public health, or similar).
2–4+ years as a Clinical Research Coordinator or similar role, ideally with longitudinal or registry/observational studies.
Demonstrated experience managing participant scheduling, consent, follow‑up, and data collection across multiple timepoints.
Working knowledge of GCP, HIPAA, and IRB requirements for human subjects research; prior completion of GCP/CITI or equivalent.
Proven ability to work independently in a remote setting, prioritize tasks, and manage a large longitudinal participant panel.
Excellent interpersonal skills and comfort conducting virtual consent discussions and check‑ins via video/phone.

Competitive hourly rate in the range of 30–40 USD/hour, depending on experience, qualifications, and location.
Contractors are not eligible for all benefits offered to full‑time employees.

Clinical Research Coordinator

Key skills