Associate Director of Biostatistics

Job Summary

Leading statistical strategy and analysis for clinical trials, the full-time Associate Director of Biostatistics will design and report on Phase I to IV studies while collaborating with cross-functional teams in a remote setting.

Key responsibilities

• Manage the statistical design and analysis of clinical trials, ensuring timely and scientifically sound statistical expertise
• Develop and review statistical analysis plans, interpret data, and oversee statistical programming efforts
• Contribute to departmental standards and practices, and participate in regulatory meetings to address statistical questions

Required qualifications

• PhD with over 4 years of experience or MS with over 6 years of experience in statistics, mathematics, or a related field
• Strong knowledge of clinical trial design, statistical methods, and drug development regulations
• Experience in oncology therapeutic areas and proficiency in SAS or R
• Expertise in statistical contributions to NDA or BLA submissions and familiarity with CDISC standards
• Demonstrated leadership abilities and excellent interpersonal skills