Associate Director - Statistics, Specialty TA (Hybrid)

📋 Description Provide expertise/lead regulatory submission and product life-cycle management strategy planning Provide statistical leadership for design, analysis and reporting for clinical or other scientific Independently develop protocols and statistical analysis plans. Represent function/department on project team(s) to provide statistical input to compound/drug Partner with other functions (Clinical, Regulatory, Patient Safety, or GMA) to create development Demonstrate extensive understanding of statistical concepts and methodology. Propose novel 🎯 Requirements Master's degree in Statistics, Biostatistics, or a highly related field with 10+ years of Strong leadership skills and experience in working/managing cross-cultural or overseas teams. Pharmaceutical or related industry knowledge required, including experience and understanding of PhD preferred. Submission experience preferred. High degree of technical competence and excellent communication skills, both oral and written. 🎁 Benefits Paid time off (vacation, holidays, sick) Medical/dental/vision insurance, 401(k) (for eligible employees) Long-term incentive programs