Research Program Integrator

Role: Research Program Integrator overseeing research activities for Caption Health's FDA-clearance of OB AI products. Responsibilities: lead cross-functional planning, execution, and communication of research projects from initiation to closure; ensure compliance with protocols, GCP, IRB, and regional regulations; develop documentation, manage budgets/contracts, facilitate IRB submissions, conduct staff training, monitor visits, and implement process improvements. Requirements: Bachelor's in life sciences or related field; 5+ years in clinical or medical device research, with patient-facing and sponsored study experience; strong GCP/regulatory knowledge; ability to build cross-functional relationships. Preferred: project management or clinical research certifications (e.g., PMP, CCRP). High-Value: medical device research, clinical project management, IRB/regulatory compliance, cross-functional team leadership. Work setup: not specified, no travel requirements noted.