Jodi Schinski

Jodi Schinski is an experienced regulatory affairs professional with a robust background in CMC (Chemistry, Manufacturing, and Controls). Currently serving as Senior Director of Regulatory Affairs CMC at Cidara Therapeutics since January 2022, Jodi has previously held the position of Director of Regulatory Affairs CMC at Merck from July 2018 to January 2022. Earlier experience includes roles as Director and Senior Manager of Regulatory Affairs at Renaissance SSA, LLC from July 2014 to July 2018, and as Manager, Senior Regulatory Affairs Specialist, Regulatory Affairs Specialist I, Associate Scientist II, and Associate Scientist I at Teva Pharmaceuticals from January 2003 to June 2014. Jodi holds a Master of Science in Cell Biology and Biotechnology from the University of the Sciences in Philadelphia and a Bachelor of Science in Biology from York College of Pennsylvania.