Research Associate 2

The Research Associate supports formation and administrative operations of Yale's Clinical Events Committee within a clinical research environment, coordinating adjudication meetings, preparing blinded endpoint packets, drafting and reviewing clinical event narratives, data verification, and ensuring timely communication among trial sponsors, clinical sites, and internal teams. Responsibilities include maintaining study master files, developing templates to support efficient workflows, QA/QC activities, identifying discrepancies, training new personnel, contributing to process improvements, and adhering to GCP and study protocols. May perform additional functions such as safety coordination and problem resolution, and collaborates with PIs on major revisions and regulatory submissions. Requires strong communication, attention to detail, organizational skills, and proficiency with Microsoft Office and clinical trial systems (EDC, CTMS). Preferred: Bachelor’s in life sciences/public health/nursing or related field (Master's preferred) with 3 years of clinical research experience; familiarity with GCP and regulatory requirements; experience with medical record review and data safety/adjudication.