About this role
Study Manager at Evvy. Location: New York City, New York, United States. Role: Oversee studies end-to-end, Manage PI and site relationships, Ensure regulatory documentation Requirements: 5–7 years coordinating multi-site clinical studies; IRB submissions; site management; ICH-GCP; HIPAA; FDA knowledge; strong organization. Category: Research and Development (R&D) Seniority: Mid Level Tools: EDC, IRB platforms, eTMF, protocols, spreadsheets, data management Commitment: Full Time Workplace: Onsite Languages: English