Associate Director, Statistical Programming

Kymera Therapeutics is seeking an experienced and strategic Associate Director of Statistical Programming to lead programming efforts across multiple clinical studies. This role will be instrumental in ensuring high-quality, timely, and compliant statistical deliverables in support of Kymera’s innovative degrader pipeline. The ideal candidate has a deep understanding of clinical trial conduct, data flow, and regulatory expectations, and is comfortable being 50% hands-on in programming. This individual will proactively identify risks, solve complex problems, and collaborate effectively with cross-functional stakeholders and external partners. Responsibilities include leading multiple studies, collaborating with internal and external partners, overseeing CRO deliverables, developing and validating datasets, providing expertise for regulatory submissions, coordinating data transfers, reviewing documents, troubleshooting issues, and staying current with industry trends.