Associate Director, Biostatistics

Responsibilities

• Develop or assist in creating study protocols and statistical analysis plans (SAPs)
• Participate in database design to ensure data quality for analysis
• Collaborate with programming staff to ensure analytical programs meet standards and regulatory requirements
• Analyze and interpret clinical trial data according to study protocols
• Prepare and present reports on clinical trial results to project teams
• Respond to inquiries regarding study design, analysis, and interpretation from regulatory agents and investigators
• Engage in research for innovative statistical methods in clinical trial development

Qualifications

• PhD in Statistics or related field with 5+ years experience, or Master's degree with 8+ years experience in clinical drug development
• Strong knowledge of SAS and/or R programming
• Experience with clinical trials and understanding of regulatory compliance are mandatory
• Excellent verbal and written communication skills are essential
• Prominent analytical thinking skills and good decision-making abilities

Benefits

• Comprehensive medical, dental, and vision insurance
• 401(k) plan with company matching contributions
• Flexible spending accounts (FSA) and health savings accounts (HSA)
• Life insurance and paid time off (PTO)
• Wellness program initiatives and support
• Equity ownership opportunities through stock options and the Employee Stock Purchase Plan