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:
Minimum Qualifications
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.
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....stakeholder management skills. Proven ability to lead teams and manage multiple projects while maintaining high standards of quality. Preferred Qualifications CTS certification Experience in government or large-scale AV integration projects. #LI-OnSite...
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