Associate Director or Director, Biostatistics

Role: Study/Program Lead Statistician driving statistical efforts in Kymera's clinical development of targeted protein degradation therapies. Responsibilities: serve as the statistical expert on clinical study/program teams, contribute to development plans, author statistical sections for protocols and reports, oversee CROs, and support regulatory submissions. Qualifications: advanced degree in Statistics or related field; at least 6 years of clinical trial experience in biotech/pharma; expertise in SAS, familiarity with R/Python and trial design software; comprehensive knowledge of FDA, EMA, and ICH guidelines. High-Value: biotech-specific focus on innovative degraders, experience leading statistical activities for biologics or small molecules in phases I-III; involvement in regulatory interactions; strong cross-functional collaboration skills. WorkSetup: not specified.