Study Manager

📋 Description Run and manage Evvy's portfolio of clinical studies end-to-end in NYC Own PI and site relationships; primary contact with PIs and clinical partner sites Manage study operations; ensure sites have materials and shipping to labs Co-lead site activation: site selection, contracting, training, monitoring Manage IRB submissions and regulatory docs Maintain clinical docs (protocols, consents, eTMF, EDC) for audits 🎯 Requirements 5-7 years coordinating clinical studies across multiple study types Multi-site or CRO experience; run studies across multiple PIs and sites AI in clinical research; applying AI to protocols and site communications Experience in women's health, OB-GYN, fertility, or microbiome IRB submission experience (WCG/Advarra/central/local) and EDC familiarity ICH-GCP, FDA, HIPAA knowledge; CCRC/CCRP/ACRP preferred 🎁 Benefits Flexible PTO $1K learning and development budget Health, dental, and vision insurance, plus HSA plans 401(k) plan (Roth and traditional) Monthly team events Paid parental leave