Associate Director, GCP/GLP/GVP QA

Role: Associate Director, GCP/GLP/GVP QA, overseeing clinical quality assurance activities to ensure compliance across Rhythm's clinical studies for rare neuroendocrine diseases. Responsibilities: provide GCP oversight, develop and manage GCP quality processes, conduct audits, manage vendor relationships, lead or support GCP inspections, review regulatory documents, and facilitate training to promote high-quality clinical programs. Qualifications: Bachelor's in a scientific field; 8+ years of industry experience, with 5+ years in GCP QA or clinical trial roles; expertise supporting GCP inspections and a comprehensive understanding of ICH GCP and global regulations. Preferred: knowledge of GLP and GVP regulations. HighValue: focus on GCP compliance within clinical development, support for complex international trials, vendor and audit management, and inspection readiness. WorkSetup: hybrid Boston, Massachusetts; up to 25% travel including international trips.