Other responsibilities include: assuming the regulatory lead for IRB protocol submissions, modifications, continuing reviews, reportable new information, and consent revisions; maintaining the study regulatory binder under single-IRB oversight at MGB, and maintaining compliance with Federal, State and sponsor (e.g., NIMH) guidelines, audits, and sponsor progress reports. Specifically, this position entails managing multiple clinical studies (e.g., including a randomized controlled trial), with day-to-day supervision and training of research coordinators and other staff, often involving multiple sites or stake-holders.