Associate Director, Nonclinical Writing

Role: Lead strategy and implementation of AI-enabled capabilities in nonclinical workflows, focusing on digital solutions to enhance productivity, data integrity, and regulatory documentation. Responsibilities: manage AI use case prioritization and ROI tracking; collaborate with scientific, regulatory, quality, IT, and business teams to deploy scalable AI tools; oversee nonclinical writing processes to improve data verification and document authoring; define AI strategy aligned with organizational innovation goals; promote responsible AI adoption across workflows; evaluate emerging AI platforms and ensure compliance with regulatory standards; develop best practices and training to sustain AI integration. Requirements: Bachelor's in a relevant scientific field; 5–10 years in AI, digital transformation, computational sciences, or nonclinical R&D; expertise in regulatory document authoring and translating scientific needs into AI solutions; proficiency with AI platforms, automation, and responsible deployment models; strong knowledge of life sciences, nonclinical data systems, and regulated environments; experience communicating with technical and senior leadership. Preferred: experience with enterprise AI tools, data architecture, cloud platforms, AI governance, vendor management, and knowledge of global health authority requirements such as ICH, OECD, SEND. HighValue: AI-enabled nonclinical workflows, regulatory document automation, responsible AI practices, cross-functional collaboration, hybrid flexible role in Cambridge, MA.