Teams at Seaport Therapeutics

Leads integrated planning and execution for a clinical-stage pharmaceutical program. Develops timelines, milestones, risk plans, dashboards, and scenarios; facilitates cross-functional program meetings; manages issues, decisions, workstreams, resources, budgets, and executive updates. The role also builds standardized program management tools, processes, and document-sharing practices across the company while partnering with clinical, regulatory, CMC, and nonclinical teams.

Lead QA activities for CMC supporting clinical GMP manufacturing and CMOs, including document and batch record review, deviations/investigations oversight, product release coordination, GMP metrics, and support for CMC regulatory submissions. Ensures compliance and timely clinical supply release while fostering continuous improvement.