Added
12 hours ago
Location
Type
Full time
Salary
Salary not provided

Related skills

data quality biostatistics clinical trials study design fda regulations

📋 Description

  • Responsible for protocol development including study design, sample size calculation
  • Provide statistical oversight to studies and assure adequate quality and consistency with project
  • Responsible for assuring that data for statistical analyses are complete, accurate, and consistent.
  • Responsible for statistical analysis plans and the accuracy and timeliness of statistical input
  • Responsible for the validity of the analysis and exploring alternative analysis strategies as
  • Demonstrates extensive understanding of statistical concepts and methodologies. Recognizes and

🎯 Requirements

  • MS or PhD in Statistics, Biostatistics, or related field. PhD with 3-4 years of experience or MS
  • There are no specific therapeutic area requirements; however, experience in Oncology, Rare Disease
  • Strong oral and written communication skills, with the ability to effectively communicate
  • Demonstrated understanding and insight in statistics, drug development process, and relevant FDA
  • Pharmaceutical, CRO, or related industry experience with clinical trials, including interaction
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 — finding, filtering, and applying while you focus on what matters.

Related Data Jobs

See more Data jobs →