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Biostatician - Clinical Trials Design and Analysis

HonorHealth
United States, Arizona, Scottsdale
9003 East Shea Boulevard (Show on map)
Jan 09, 2026
Overview Looking to be part of something more meaningful? At HonorHealth, you'll be part of a team, creating a multi-dimensional care experience for our patients. You'll have opportunities to make a difference. From our Ambassador Movement to our robust training and development programs, you can select where and how you want to make an impact. HonorHealth offers a diverse benefits portfolio for our full-time and part-time team members designed to help you and your family live your best lives. Visit honorhealth.com/benefits to learn more. Join us. Let's go beyond expectations and transform healthcare together. HonorHealth is one of Arizona's largest nonprofit healthcare systems, serving a population of five million people in the greater Phoenix metropolitan area. The comprehensive network encompasses six acute-care hospitals, an extensive medical group with primary, specialty and urgent care services, a cancer care network, outpatient surgery centers, clinical research, medical education, a foundation, an accountable care organization, community services and more. With nearly 17,000 team members, 3,700 affiliated providers and close to 2,000 volunteers dedicated to providing high quality care, HonorHealth strives to go beyond the expectations of a traditional healthcare system to improve the health and well-being of communities across Arizona. Learn more at HonorHealth.com. Responsibilities Job SummaryThe Post-Doctoral Fellow or Early-Stage Researcher in Clinical Trials Design and Analysis contributes to the development, implementation, and evaluation of innovative clinical trial methodologies. This role supports the HonorHealth Research Institute's mission to advance evidence-based care through rigorous research. The Fellow/Researcher will design and analyze trials using both traditional and precision-based frameworks, collaborate with interdisciplinary teams, and disseminate findings through publications and presentations. Essential Functions Design clinical trials using diverse methodologies including RCTs, crossover, sequential, bucket, and umbrella trials. Develop and execute statistical analysis plans aligned with trial objectives and regulatory standards. Contribute to IRB protocol development and ensure compliance with ethical and regulatory requirements. Collaborate with clinicians, data scientists, and regulatory experts to implement and analyze trials. Publish research findings in peer-reviewed journals and presents at scientific conferences. Stay current with emerging trends in trial design, precision medicine, and statistical innovations. Mentor junior researchers and contribute to internal knowledge-sharing initiatives. Education Ph.D. in biostatistics, statistics, mathematics, or related discipline. - Required Post-doctoral training in clinical research or trial design. - Preferred Experience Demonstrated expertise in clinical trial design and analysis; publication record in peer-reviewed journals. - Required Industry experience; exposure to adaptive designs, Bayesian methods, or machine learning in trials. - Preferred License and Certifications