Associate Director - Statistics, Specialty TA (Hybrid)

Added
6 hours ago
Type
Full time
Salary
Upgrade to Premium to se...

Related skills

statistics regulatory affairs biostatistics clinical trials pharmaceutical industry

πŸ“‹ Description

  • Provide expertise/lead regulatory submission and product life-cycle management strategy planning
  • Represent function/department on project team(s) to provide statistical input to compound/drug
  • Demonstrate extensive understanding of statistical concepts and methodology. Propose novel
  • Train and mentor staff on statistical methodology and operations. May supervise contract
  • Develop strategy for data presentation and inference. Ensure appropriate interpretation of
  • Act as the liaison for statistical issues on collaborative studies with CROs, academic

🎯 Requirements

  • MS (with 10+ years of experience) or PhD (with 6+ years of experience) in Statistics
  • Have strong leadership skills and experience in managing cross-cultural or overseas teams.
  • Pharmaceutical or related industry knowledge required, including experience and understanding of
  • Excellent communication and technical skills.
  • Ability to identify data and analytical issues, and assist with providing solutions by applying own
  • Ability to manage project timelines and quality of high quality deliverables.

🎁 Benefits

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

Meet JobCopilot: Your Personal AI Job Hunter

Automatically Apply to Data Jobs. Just set your preferences and Job Copilot will do the rest β€” finding, filtering, and applying while you focus on what matters.

Related Data Jobs

See more Data jobs β†’