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Biostatistician II

University of Southern California
$104, 390
United States, California, San Diego
Feb 07, 2026

The USC Keck School of Medicine Epstein Family Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California, is an academic institute of internally renowned scientific collaborators committed to advancing the development of new treatments for Alzheimer's Disease and related dementias (ADRD) through innovative, multi-site clinical studies, including clinical trials. The ATRI Biostatistics Section provides the biostatistical leadership for all clinical studies managed by the Institute.

This Biostatistician II will join a well-established group of statisticians and actively contribute to the Institute's work and mission. With moderate supervision, this individual will apply intermediate to advanced statistical methods and extensive statistical programming in the software to support the analysis, interpretation, and reporting of complex ADRD clinical research data. This role includes serving as thelead statistical analyst for assigned AD clinical trials, with responsibility for statistical programming of analysis and study reports, and contributing to statistical oversight across the trial lifecycle in close collaboration with the section biostatistics unit faculty and leadership. The Biostatistician II will contribute communicate regularly with internal and external collaborators, and organize and maintain confidential project materials. A successful candidate is a collaborative team member with experience in ADRD trials and who demonstrates the ability to take on increasing leadership and analytical responsibility over time.

Education and Experience

  • Master's degree in biostatistics or statistics
  • 3-4 years of working experience with sustained excellent performance post degree
  • Prior experience supportingADRD or related neurodegenerative clinical trialsis strongly preferred

Requirements:

  • Extensive statistical programming experience in R, including development of analysis-ready datasets
  • Strong knowledge of standard and advanced statistical methods
  • Demonstrated experience with clinical trials, including longitudinal data
  • Ability to serve as serve as alead statistical analyston assigned AD clinical trials
  • Ability to direct and promote teamwork within a multidisciplinary research enviroment
  • Demonstrated initiative, motivation, and attention to detail
  • Excellent written and verbal communications skills
  • Strong organizational skills and ability to manage multiple priorities
  • Ability to adapt to evolving project needs and timelines
  • Positive attitude and ability to work effectively and collaboratively with others

The annual base salary range for this position is $104, 390.76 -$132,636.23. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.

USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying.


Minimum Education:
Master's degree Or
Master's degree Biostatistics Or
Master's degree Statistics Or
Master's degree in related field(s) Or
Additional Education Requirements
Combined experience/education as substitute for minimum education
Minimum Experience:
3 years
Minimum Skills:
Experience in biostatistics, statistics, biometry or related field.
Experience in statistical programming using standard statistical packages (e.g., SAS, R, STATA).
Working knowledge of regulatory Data Standards (e.g., CDISC/ADaM).
Knowledge of clinical research regulatory requirements (e.g., Good Clinical Practice [ICH / GCP], FDA / CFR).
Ability to interact productively as part of a research team.
Ability to present ideas clearly and effectively, both orally and in writing.
Preferred Education:
Master's degree
Preferred Experience:
5 years
Preferred Skills:
Prior experience as a biostatistician in a medical research environment.
Job ID REQ20171719
Posted Date 02/06/2026
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