Remote Biostatistician

Summary

Join our team as a Biostatistician at Endpoint Clinical, where you'll be responsible for statistical analysis and interpretation of clinical trial data, working closely with cross-functional teams to ensure accurate and meaningful results.

Requirements

• Master’s or PhD in Statistics, Biostatistics, or a related field is required
• Bachelor’s degree with substantial working experience in biostatistics will be considered
• 2+ years of biostatistics experience, preferably in clinical trials
• Proficiency in statistical software such as SAS, R, or Python required

Responsibilities

• Provide statistical expertise in the design and analysis of clinical trials
• Develop and author Statistical Analysis Plans (SAPs) for assigned projects
• Review clinical trial protocols to ensure statistical soundness and provide feedback to study teams
• Author the protocol statistical sections and generate SAPs and study randomization
• Analyze clinical trial data using advanced statistical techniques and software
• Collaborate closely with Statistical Programmers to review and validate data sets, tables, listings, and other statistical outputs
• Review and sign-off on relevant study documents and data management and programming deliverables
• Provide programming support to supplemental or exploratory analyses any other internal and external ad-hoc requests
• Stay current with relevant regulatory guidelines and ensure compliance in all statistical deliverables
• Represent the biostatistics function on project teams and in cross-functional meetings
• Perform other duties as required and assigned

Preferred Qualifications

Experience in the life sciences, regulatory environments, and knowledge of 21 CFR Part 11 and GxP is highly preferred

Benefits

• Medical
• Dental
• Vision
• Life
• STD/LTD
• 401(K)
• Paid time off (PTO) or Flexible time off (FTO)
• Company bonus where applicable