Biostatistician I

Usc (Externalusccareers)

San Diego (CA)

On-site

USD 86,000 - 109,000

Full time

7 days ago
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Job summary

The USC Keck School of Medicine, Epstein Family Alzheimer Therapeutic Research Institute (ATRI) in San Diego is seeking a Biostatistician I to contribute to clinical trial statistics, data management, and reporting under senior guidance.

The role focuses on statistical programming in R, longitudinal analyses, and collaboration with investigators, with increasing responsibility as expertise grows, and requires on-site presence three days per week.

Qualifications

  • Master’s degree in biostatistics or statistics.
  • 1–2 years of relevant professional research experience following the graduate degree.
  • Strong training in statistical theory and methods.
  • Excellent R programming skills and ability to implement analyses within an established framework.
  • Experience analyzing longitudinal or other complex research data.

Responsibilities

  • Perform statistical programming and analyses for clinical trials under guidance.
  • Apply appropriate statistical methods to longitudinal and other trial data.
  • Prepare, manage, and evaluate analysis-ready datasets and outputs.
  • Contribute to QC/QA of analyses and programming.
  • Contribute to statistical methods, reports, and manuscripts.
  • Communicate statistical methods and results clearly to multidisciplinary collaborators.
  • Develop understanding of assigned studies including design and data structure.
  • Manage assigned projects with high standards for accuracy and reproducibility.
  • Seek guidance from senior staff when addressing complex issues.
  • Take initiative and increase responsibility with experience.

Skills

R programming
Statistical theory

Education

Master's degree in biostatistics or statistics

Tools

R
SAS
STATA

Job description

The USC Keck School of Medicine, Epstein Family Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California, is an academic institute focused on advancing the development of treatments for Alzheimer’s Disease (AD) and related dementias through innovative clinical trials. The ATRI Biostatistics Section provides the statistical leadership for all clinical trials and studies managed by ATRI.

We are seeking a highly trained and motivated Biostatistician I with strong statistical programming and quantitative skills who is interested in developing a career in clinical trials biostatistics in an academic research environment. This position is particularly suited to an early-career biostatistician who already has a strong foundation in statistical methodology and programming and is prepared to contribute substantively to clinical research from the outset.

The Biostatistician I will join an established group of statisticians and work closely with the section biostatisticians, study investigators and other research collaborators. The individual will work under the direction of senior biostatistics staff and faculty biostatisticians, with statistical guidance and oversight provided as part of each assigned clinical trial or study. The Biostatistician I will be an integral member of the study team and will not be expected to independently provide statistical leadership for a clinical trial. The individual will develop an in-depth understanding of assigned clinical trials and will take on progressively greater statistical responsibility as their experience and expertise develop.

The Biostatistician I will:

  • Perform statistical programming and analyses for clinical trials and related research studies under the direction of senior biostatistics staff and faculty biostatisticians.
  • Apply appropriate statistical methods to longitudinal and other clinical trial data.
  • Prepare, manage, and evaluate analysis-ready datasets and statistical outputs.
  • Contribute to quality control and quality assurance of statistical analyses and programming.
  • Contribute to statistical methods, analysis descriptions, reports, presentations, and scientific manuscripts.
  • Clearly communicate statistical methods and results to statisticians, investigators, and multidisciplinary collaborators.
  • Develop a detailed understanding of assigned studies, including study design, data structure, analysis objectives, and statistical responsibilities.
  • Manage assigned projects effectively while maintaining high standards for accuracy, reproducibility, documentation, and organization.
  • Seek appropriate statistical guidance and work collaboratively with senior biostatistics staff when addressing complex statistical or study-specific issues.
  • Take initiative, work collaboratively, and assume increasing responsibility as knowledge and experience develop.
Education and Experience
  • Master’s degree in biostatistics or statistics
  • 1–2 years of relevant professional research experience following the graduate degree.
Requirements:
  • Strong training in statistical theory and methods.
  • Excellent R programming skills and demonstrated ability to implement statistical analyses with a high degree of technical independence within an established statistical analysis framework
  • Experience analyzing longitudinal or other complex research data.
  • Strong written and verbal communication skills, including the ability to explain statistical concepts and results clearly to multidisciplinary collaborators.
  • Strong attention to detail, organization, and commitment to high-quality, reproducible statistical work.
  • Ability to work effectively within a collaborative biostatistics team, independently manage assigned responsibilities, and seek guidance appropriately from senior biostatistics staff.
  • Initiative and ability to adapt to changing priorities.
Strongly preferred:
  • Experience supporting clinical trials or clinical research.
  • Familiarity with clinical trial design, analysis, and reporting.
  • Demonstrated interest in developing a long-term career in academic clinical trials biostatistics.
  • Experience contributing to scientific reports, presentations, abstracts, or manuscripts.
Work Location

This position requires regular on-site presence at ATRI in San Diego three days per week. Candidates should apply with the expectation that this is an ongoing requirement of the position.

Compensation

The annual base salary range for this position is $85,894.21 - $108,687.46. 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.

Career Development

This position is designed for a biostatistician who wants to build expertise in Alzheimer’s disease clinical trials and progressively take on greater statistical responsibility. The Biostatistician I will work closely with experienced senior biostatistics staff and faculty biostatisticians while developing deeper expertise in clinical trial design, analysis, and reporting. Successful Biostatistician I staff are expected to demonstrate increasing independence in statistical programming, analysis, communication, and study responsibilities as they gain experience.

USC Fair Chance Statement

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, Combined experience/education as substitute for minimum education

Minimum Experience: 1 year, Combined education/experience as substitute for minimum experience

Minimum Field of Expertise: Experience in Biostatistics , Statistics or related field . Experience with SAS, R or STATA.

USC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. 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.

We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone at (213) 821-8100, or by email at uchr@usc.edu. Inquiries will be treated as confidential to the extent permitted by law.

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