Director of Biostatistics at Tempus leading a team focused on clinical research. Collaborating across departments, driving regulatory submissions, and developing statistical analysis plans.
Responsibilities
Build and lead a high-performance team of biostatisticians
Provide expert conceptual and methodological leadership
Lead development on statistical analysis plan (SAP)
Drive the planning and delivery of key analytical or clinical components of regulatory submissions
Collaborate with data scientists, laboratory scientists, the medical team, technologists and the regulatory team on study design and analysis
Produce high-quality documentation for all projects
Stay updated on the latest methodological advances in real world data studies
Comply with all regulations and Company procedures
Requirements
Ph.D. or Masters Degree in Biostatistics, Statistics, or a related field with 7+ years (Ph.D.) / 9+ years (MS/MA) relevant industry experience
Proven experience working with Real World Data and its applications in clinical research
Experience developing SOPs to document departmental processes for biostatistics
Demonstrated management skills; ability to manage the work of Ph.D./MS level biostatisticians
Experience working with other groups involved in clinical research, such as Statistical Programmers, Clinical Operations, Data Managers
Thorough understanding of statistical principles and clinical experiment methodology
Computational skills using R, and/or SAS
Ability to work in a multi-disciplinary team setting
Able to prioritize and manage several projects simultaneously
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