Biostatistics Associate Director

Job Summary

Leading statistical research tasks, the full-time Associate Director of Biostatistics will plan and analyze patient-reported outcomes in clinical trials and real-world data, develop statistical analysis plans, and collaborate with multidisciplinary teams, with the option to work remotely or in a hybrid setting, preferably from North Carolina.

Key responsibilities

• Plan, conduct, and document statistical analyses for clinical trials and observational studies, focusing on patient-reported outcomes
• Develop statistical analysis plans and contribute to the writing of study reports, protocols, and proposals
• Mentor less experienced staff and ensure the quality and timeliness of statistical analyses and outputs

Required qualifications

• Master's degree with at least 6 years of experience, or PhD with at least 1 year of experience, or equivalent combination of education and experience
• Demonstrated programming skills in SAS, including developing reproducible analysis pipelines
• Experience analyzing patient-reported outcome data in clinical trials
• Background in biostatistics or related quantitative disciplines
• Knowledge of Good Clinical Practice (GCP) and regulatory environments