Associate Director - Statistics, Specialty TA (Hybrid)

Role: Associate Director of Statistics leading statistical strategies for clinical development and lifecycle management of biopharma projects. Primary focus includes designing, analyzing, and reporting clinical trials, with an emphasis on regulatory submissions and scientific research programs. Responsibilities encompass developing protocols and analysis plans, providing statistical input to cross-functional teams, mentoring staff, and ensuring regulatory compliance. The role also involves proposing innovative statistical methods, collaborating with CROs and external partners, and supporting publications and regulatory discussions. Qualifications: MS with 10+ years or PhD with 6+ years in Statistics, Biostatistics, or related fields; experience in the pharmaceutical industry, drug development, and lifecycle management within regulated environments essential. Preferred: PhD and prior submission experience. Skills include strong technical expertise, excellent communication, project management, and cross-functional relationship building. High-value details: focus on clinical trials, regulatory submissions, and lifecycle strategies in a regulated biopharma setting, with expertise in statistical methodologies and compliance. The position may involve collaboration with external partners and requires leadership skills. Location: not specified, likely flexible based on company policy.