Associate Director, IT Regulatory, Clinical, and Enterprise Systems
Core
Lead digital processes and IT systems for Clinical Operations, Regulatory, and Supply Chain Planning to enable commercialization of radiopharmaceutical therapies.
Role type
Senior IT Program Director (Regulatory & Clinical Systems)
Builds
Regulated digital solutions, service level management, and long-term technology roadmaps for clinical and regulatory functions.
Domain
Biotechnology / Radiopharmaceuticals / Regulated IT
Required skills
IT leadership in cGMP/Radiopharmaceutical environments, budget management, strategic roadmap planning, vendor management, risk-based validation, stakeholder influence, AI application for team execution.
Preferred skills
Experience with clinical site portals, RIM, supply chain planning systems, disaster recovery planning, architectural partnership.
Technologies
Clinical site portal, RIM, supply chain planning systems, AI tools.
Responsibilities
Ensure continuous operation of regulated digital solutions; deliver service level management and disaster recovery; lead indirect reports and service providers; partner with functional leaders on process automation; provide IT leadership for regulatory inspection readiness; manage long-term technology roadmaps; apply AI to improve team execution.
Seniority
Senior, hands-on IC with management responsibilities