I'm looking for someone with experience managing regulatory operations with strong submissions experience. This person will work on one of the industry's most anticipated oncology products. This opportunity is with a growing oncology/hematology company with locations in Orange County, CA, and Cambridge, MA. As a whole, this company has multiple, late-phase, novel oncology molecules as well as an early phase I/O pipeline. This person will manage the compilation and production of various regulatory submissions for biologic and small molecule products.

This company offers an excellent all-encompassing compensation package with base, bonus, stock, LTIs, and strong benefits. If interested in learning more, I'm widely available between 11 am - 8 pm EST this week and next. Please apply today!