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Remote Clinical Research Regulatory Coordinator
Mariposa Medical • Remote, US • published 2026-11-03 03:17:06.344990
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About Us Amari is a multi\-specialty clinical research site conducting Phase 2–4 industry\-sponsored trials in allergy, asthma, immunology, and respiratory medicine. We work with leading pharmaceutical sponsors and CROs and are known for our high\-quality data, strong enrollment, and inspection\-ready operations. Position Summary We are seeking an experienced Regulatory Coordinator to manage the full regulatory lifecycle of our clinical trial portfolio. This is a fully remote role, part time contractor role, for a seasoned professional who can independently maintain the site’s electronic Investigator Site Files (eISF), manage IRB submissions, and keep every study audit\- and inspection\-ready at all times. Key Responsibilities **Study start\-up** * Prepare, collect, and submit essential regulatory documents (FDA 1572, financial disclosures, CVs, medical licenses, GCP and training certificates, delegation logs) to sponsors and CROs * Complete feasibility questionnaires, site qualification packets, and vendor access requests * Coordinate initial IRB submissions with central IRBs (Advarra, WCG) and local IRBs as needed **eISF management (Veeva Vault / SiteVault, CRIO, RealTime, and/or...
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