Systimmune
Biostatistician - python / sap / clinical trials at Systimmune Redmond, WA
Systimmune, Redmond, Washington, United States, 98052
Biostatistician - Python / SAS / Clinical Trials job at SystImmune. Redmond, WA.
Job Description
SystImmune Inc. is a clinical-stage biopharmaceutical company located in Redmond, WA. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has several assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a strong preclinical pipeline of potential cancer therapeutics in discovery or IND-enabling stages, representing cutting-edge biologics development. Position Objective: The biostatistician will collaborate with senior biostatisticians on clinical or non-clinical studies. The successful candidate will leverage data science and statistical expertise to support data cleaning, visualization, analysis, and reporting for new drug discovery efforts. Main Job Responsibilities: Provide data-driven insights and statistical support to clinical teams, offering guidance on data challenges and participating in project meetings. Collaborate on study design and clinical study protocols. Develop, validate, and maintain programs (e.g., SAS, Python, R) for data analysis to generate tables, listings, and figures. Conduct interim analyses, including statistical and pharmacokinetics analyses, to support clinical decisions. Develop and review Statistical Analysis Plans (SAP), and review final study reports and submissions. Oversee and validate CRO programming activities, ensuring accuracy in SDTM, ADaM, and other data standards. Ensure quality control of project deliverables, maintaining data integrity and reporting standards. Perform simulations and ad-hoc statistical analyses as needed. Understand and apply regulatory guidelines and industry standards in statistics and programming. Qualifications: Master’s Degree or PhD in Biostatistics, Statistics, or related field. 3+ years of statistical work experience. Proficiency in statistical programming languages such as SAS, R, Python. Experience with CDISC and CDASH standards. Strong knowledge of clinical trial design, data analysis, and ability to communicate statistical concepts. Knowledge of applied statistics, including regression, categorical data, and survival analysis. Understanding of clinical research, drug development, and medical terminology; oncology experience preferred. Excellent communication and presentation skills. Benefits: SystImmune offers a stable, well-funded environment with opportunities for growth. Benefits include: 100% paid premiums for medical/dental/vision, STD, LTD, a 401(k) plan with 50% company match up to 3%, 15 PTO days, sick leave, 11 paid holidays, and more. Equal Opportunity Employer Powered by JazzHR RgR46exc2X
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SystImmune Inc. is a clinical-stage biopharmaceutical company located in Redmond, WA. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has several assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a strong preclinical pipeline of potential cancer therapeutics in discovery or IND-enabling stages, representing cutting-edge biologics development. Position Objective: The biostatistician will collaborate with senior biostatisticians on clinical or non-clinical studies. The successful candidate will leverage data science and statistical expertise to support data cleaning, visualization, analysis, and reporting for new drug discovery efforts. Main Job Responsibilities: Provide data-driven insights and statistical support to clinical teams, offering guidance on data challenges and participating in project meetings. Collaborate on study design and clinical study protocols. Develop, validate, and maintain programs (e.g., SAS, Python, R) for data analysis to generate tables, listings, and figures. Conduct interim analyses, including statistical and pharmacokinetics analyses, to support clinical decisions. Develop and review Statistical Analysis Plans (SAP), and review final study reports and submissions. Oversee and validate CRO programming activities, ensuring accuracy in SDTM, ADaM, and other data standards. Ensure quality control of project deliverables, maintaining data integrity and reporting standards. Perform simulations and ad-hoc statistical analyses as needed. Understand and apply regulatory guidelines and industry standards in statistics and programming. Qualifications: Master’s Degree or PhD in Biostatistics, Statistics, or related field. 3+ years of statistical work experience. Proficiency in statistical programming languages such as SAS, R, Python. Experience with CDISC and CDASH standards. Strong knowledge of clinical trial design, data analysis, and ability to communicate statistical concepts. Knowledge of applied statistics, including regression, categorical data, and survival analysis. Understanding of clinical research, drug development, and medical terminology; oncology experience preferred. Excellent communication and presentation skills. Benefits: SystImmune offers a stable, well-funded environment with opportunities for growth. Benefits include: 100% paid premiums for medical/dental/vision, STD, LTD, a 401(k) plan with 50% company match up to 3%, 15 PTO days, sick leave, 11 paid holidays, and more. Equal Opportunity Employer Powered by JazzHR RgR46exc2X
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