Biostatistician

Job Summary

A company is looking for a Biostatistician to support drug development and regulatory submissions in a remote setting.

Key Responsibilities

• Design and analyze clinical trials and contribute to the clinical development plan
• Collaborate with cross-functional teams to deliver statistical components for clinical trials and regulatory submissions
• Lead and monitor statistical activities across multiple clinical trials

Required Qualifications

• 5+ years of relevant experience in biostatistics and drug development
• Proficiency in statistical software such as SAS and/or R
• Experience with regulatory submissions and knowledge of eCRT and Define standards
• Masters or PhD in Statistics or a related field
• Preferably experienced in Immunology and familiar with modern statistical models