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

• MS with 10+ years of experience or PhD with 6+ years of experience in Statistics, Biostatistics, or
• Strong leadership skills and experience working/managing cross-cultural or overseas teams.
• Pharmaceutical or related industry knowledge; experience with drug development and life-cycle
• Excellent communication skills (oral and written)
• Ability to identify data or analytical issues and provide solutions.
• Skill in managing project timelines and quality of deliverables.

🎁 Benefits

• Comprehensive package of benefits including paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance
• 401(k) eligibility
• Participation in long-term incentive programs