EXEC DIR REGULATORY -CMC

The strategic Executive Director of Regulatory Affairs will report to the SVP/VP/Head of

Regulatory Affairs and will be responsible for leading the overall CMC regulatory strategy for

gene therapy programs. This individual will be the key interface between the

Regulatory and CMC functions, partner with Process Development, Manufacturing, Supply Chain, and Quality; and assist in ensuring regulatory compliance. The Executive Director will be responsible for developing, executing, and advising on global Regulatory CMC strategies through all phases of development programs. This individual may interface with business partners, as appropriate, in regard to development, regulatory, and registration strategies.