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.

🎯 Requirements

• MS (with 10+ years of experience) or PhD (with 6+ years of experience) in Statistics
• Strong leadership skills and experience in working/managing cross-cultural or overseas teams
• Pharmaceutical or related industry knowledge, including experience and understanding of drug
• High degree of technical competence and excellent written and oral communication skills
• Ability to identify data or analytical issues, and provide solutions by applying own skills or
• Ability to manage project timeline and quality of deliverables

🎁 Benefits

• Pay
• Paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance
• 401(k)
• Long-term incentive programs