Director, Site and CMC Program Management

Role: Lead strategic and operational project management for CMC programs at the Indianapolis site within a biotech focused on radiopharmaceuticals for oncology. Responsibilities: serve on site leadership, build and oversee program management capabilities, coordinate across functions like process development, supply chain, manufacturing, quality, and regulatory; translate strategic priorities into detailed plans, timelines, and risk mitigation; manage site-based and cross-functional program execution including manufacturing readiness and technology transfer; develop and lead a program management team, define tools, standards, and governance routines; communicate effectively with senior stakeholders and external partners. Requirements: bachelor’s degree in life sciences, chemistry, engineering, or related field; 10+ years in pharma/biotech with experience in CMC, manufacturing, or site operations; proven leadership in cross-functional program delivery; strong understanding of drug development, CMC, supply chain, and radiopharmaceutical modalities; excellent communication, stakeholder management, and strategic planning skills. Preferred: advanced degree, prior success building program management systems, and experience supporting radiopharmaceutical or oncology product development. High-Value: oncology, radiopharmaceuticals, CMC, process development, supply chain, manufacturing, regulatory interface, site leadership, cross-functional collaboration. Work setup: primarily office-based with occasional travel.