The University of Southern California (USC), founded in 1880, is the largest private employer in the City of Los Angeles. As an employee of USC, you will be a part of a world-class research university and a member of the "Trojan Family," which is comprised of the faculty, students and staff that make the university what it is.

We are looking for a highly motivated and qualified candidate with three years’ experience in biostatistics, statistics, biometry, or a related field.  He/she will be responsible for working with investigators on the design and analysis plan of clinical studies, conduct statistical analysis of study data, and collaborate on the interpretation and reporting of the study results to be incorporated into reports, publications, and presentations. Assists with training groups and individuals on the proper use and interpretation of clinical statistics, use of statistical software programs, research design, and other research related topics. Works independently or under the direction of a Senior Biostatistician and CISO IIT management supervisor.

The following are the specific job functions:

Collaborates with the Principal Investigator (PI) and study team on various research projects in study design, conduct and analysis.

Develops project analysis plan, including computer-generated table specifications,

statistical analysis plan, and research report format.

Independently performs statistical analyses of clinical datasets with the use of

appropriate and relevant statistical methods.

Collaborates with study team in database design and management for assigned projects.

Interprets data. Prepares and disseminates project/study summaries, as required.

Prepares reports for various USC NCCC and CISO Committees, e.g. DSMC.

Supports and advises researchers within the university with statistical aspects of

studies, including external grant applications where statistical support is required.

Assists researchers in verification of correct statistical output.

Prepares reports, publications and presentations for academic and non-academic audiences.

Trains and assists in the orientation of new statistical staff.

Participates in regularly scheduled meetings with study investigators and teams.

Maintains awareness and knowledge of current changes within legal, regulatory,

and technology environments by reading journals and other pertinent publications, and participating in professional organizations, meetings, and seminars, as required.

Performs other related duties as assigned or requested. The university reserves the right to add or change duties at any time.

Minimum Qualifications

Master’s Degree in Biostatistics, Statistics, or a related field is required.Three years’ experience in biostatistics, statistics, biometry, or a related field is required.

Special Instructions to Applicants

Applicant Attachments (Required): Resume

Applicant Attachments (Optional): Cover Letter

The annual base salary range for this position is $108,768.37 - $109,000.08. 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.

The University of Southern California strongly values diversity and is committed to equal opportunity in employment.  Women and men, and members of all racial and ethnic groups, people with disabilities, and veterans are encouraged to apply.

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.