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