Senior Real World Statistics Contractor-Remote

Overview

Role involves statistical work on observational studies and clinical trials.

Ideal candidate has 3-7 years experience in biostatistics with strong programming skills in SAS and R.

Locations

• United States

Requirements

• Master or PhD in Biostatistics or related fields
• 3 to 7 years relevant experience
• 2 years in observational studies
• 3 years SAS and R programming experience

Responsibilities

• Perform statistical work for observational studies
• Collaborate with stakeholders
• Contribute to study reports and publications
• Participate in Study Execution Team meetings
• Support development of study documents
• Provide input into programming specifications