Director, IT R&D Business Partner

Role: Serve as IT strategic and operational leader supporting GxP-regulated systems in Quality, Regulatory, Clinical, and Research functions during pivotal drug development phases. Responsibilities: manage and maintain R&D business systems, oversee documentation control, ensure compliance and audit readiness, support system upgrades, troubleshoot issues, oversee vendor qualification, and drive continuous process improvements. Requirements: Bachelor's Degree or 10+ years in life sciences IT; deep knowledge of GxP regulations, quality systems, audit procedures, and laboratory/instrumentation IT; strong communication skills; experience with electronic document systems (e.g., Veeva Vault, SharePoint), and familiarity with AI, security, and governance. Preferred: experience in a fast-paced, biotech environment, advanced MS Office skills, and working knowledge of GxP concepts. HighValue: supporting clinical and regulatory systems during Phase 3 trials, ensuring compliance, scalability, and security for drug development infrastructure. WorkSetup: remote US-based; no travel specified.