Description
Evvy is hiring a Study Manager to run and manage its portfolio of observational and interventional clinical studies from site activation and IRB submissions through enrollment, monitoring, and close-out. The role owns PI and clinical partner relationships, study operations, regulatory documentation, clinical data systems, study design input, reporting, and operational playbooks. It is primarily in-person in New York City with occasional travel to clinical partner sites, and requires 5–7 years of clinical study coordination experience, including multi-site or CRO experience, IRB submission experience, and familiarity with EDC platforms.
