Statistical Research Associate I/II
Listed on 2025-12-04
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Research/Development
Clinical Research, Research Scientist -
Healthcare
Clinical Research
Overview
Fred Hutchinson Cancer Center is an independent, nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. Based in Seattle, Fred Hutch is the only National Cancer Institute-designated cancer center in Washington.
With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world’s leading cancer, infectious disease and biomedical research centers. Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states.
Together, our fully integrated research and clinical care teams seek to discover new cures to the world’s deadliest diseases and make life beyond cancer a reality.
At Fred Hutch we value collaboration, compassion, determination, excellence, innovation, integrity and respect. Our mission is directly tied to the humanity, dignity and inherent value of each employee, patient, community member and supporter. Our commitment to learning across our differences and similarities make us stronger. We seek employees who bring different and innovative ways of seeing the world and solving problems.
SWOG is a national clinical trials cooperative group funded by the National Cancer Institute. The Statistical Research Associate (SRA) is a member of the statistical team of the SWOG Cancer Research Network Statistics and Data Management Center (SDMC) in the Public Health Sciences Division. The primary activities of the SWOG SDMC include
1) the design, implementation and analysis of clinical trials that assess therapeutic interventions for all types of adult cancers as well as cancer control and prevention trials;
2) support of translational research to target markers of disease prognosis and treatment prediction; and
3) development of methodology to improve clinical trials design.
SWOG Statistical Research Associate I/II
Under supervision, the incumbent performs a variety of duties related to the statistical aspects of clinical trials or other research studies including review of trial/study design, development, implementation, monitoring, and statistical analysis using standard statistical software.
Statistical Research Associate I- Provide support in the development of the statistical aspects of protocol development and implementation.
- Support the development the study-specific data collection forms.
- Assist in the development and coordination of the quality assurance procedures for on-going data collection and analysis.
- Assist the study team with the implementation of the study in the electronic data management system.
- Provide active monitoring of ongoing clinical trials.
- Prepare written summaries and tables of results for scientific reports and papers.
- Produce semi-annual study reports.
- Provide statistical analysis of clinical trial data using statistical software programs.
- Prepare and document data for archiving and data sharing.
- Perform other duties as necessary.
In addition to the job duties of Statistical Research Associate I:
- Provide input in the development of an analysis plan of translational medicine endpoints and implement the analysis plan.
- Present at meetings including oral presentations of trial results, trial design or aspects of trial implementation.
- Master's degree in Biostatistics or Statistics.
- Background in statistical computing.
- Familiarity with statistical packages used within the department/project.
- This classification is intended as entry level for newly graduated MS statisticians or those having minimal (6-12 months) related experience.
All minimum qualifications of Statistical Research Associate I, plus:
- Minimum of one year of related experience.
- Background in statistical computing.
- Proficiency with the statistical packages used within the department/ project.
- Two years of related experience in clinical trials.
- Understanding…
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