Chromatin dynamics modulate DNA repair factor accessibility throughout the DNA damage response. The spatiotemporal scale upon which these dynamics occur render them invisible to live cell imaging. Here we employ fluorescence lifetime imaging microscopy (FLIM) for FRET detection of nucleosome arrangement in live cells and monitor the structural rearrangements of chromatin during DNA repair. With this technology we demonstrate that genomic double strand breaks induce both local and global condensation events in the chromatin network and the detected chromatin dynamics facilitate DNA repair factor recruitment specifically to the lesion site.