Associate Director, IT Regulatory, Clinical, and Enterprise Systems
Core
Lead digital solutions and IT infrastructure for Clinical Operations, Regulatory, and Supply Chain Planning to enable commercialization of radiopharmaceutical therapies.
Role type
Senior IT Program Director / Associate Director
Builds
Digital systems roadmap, automated processes, and stable IT infrastructure for regulated biotech functions
Domain
Biotechnology / Radiopharmaceuticals / Clinical Operations / Regulatory Affairs
Required skills
IT leadership in cGMP/Radiopharmaceutical environments, digital transformation, budget management, strategic roadmap planning, vendor management, risk-based validation, stakeholder influence
Preferred skills
AI application for team execution, multi-disciplinary project leadership, technology trend identification
Technologies
Clinical site portals, RIM, supply chain planning systems, regulated functional solutions
Responsibilities
Manage continuous operation of digital solutions for Clinical, Regulatory, and Supply Chain; ensure digital roadmap alignment with business outcomes; lead indirect reports and service providers; partner with functional leaders on process automation; provide IT leadership for regulatory inspection readiness and data integrity; manage new demand and evolve digital solutions; develop long-term technology roadmaps
Seniority
Senior, hands-on IC with management responsibilities