SystImmune
SystImmune is a leading and well‑funded clinical‑stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bispecific, multispecific antibodies, and antibody‑drug conjugates (ADCs). With multiple assets in various stages of clinical trials for solid tumor and hematologic indications, SystImmune also maintains a robust preclinical pipeline of potential cancer therapeutics in the discovery and IND‑enabling stages, representing cutting‑edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
Location This position requires a full‑time onsite presence at our Redmond, WA office location. Working some evenings may be required for collaboration and meetings with teams in China.
Responsibilities
Provide data‑driven insights and statistical support to clinical teams, offering guidance on data‑related challenges and participating in project team meetings as needed
Collaborate with clinical teams on study design and clinical study protocol development
Develop, validate, and maintain programs (e.g., SAS program) and conduct comprehensive data analysis using SAS, R, or other statistical software to generate TLFs as needed
Conduct and interpret interim analysis, including statistical and pharmacokinetics analysis, to support clinical decision making
Develop and review SAP, including table/listing/figure shells, and review final SAR and CSR
Oversee and validate CRO programming activities, ensuring accuracy in internally or externally produced SDTM, ADaM, SAS tables, listings, and figures
Conduct quality control of project deliverables, ensuring compliance with data integrity and reporting standards
Perform simulations and ad‑hoc statistical analysis when needed
Understand and apply regulatory guidelines and industry standards practices on statistics and SAS programming
Qualifications
Master’s Degree with 3+ years of statistical work experience or PhD in Biostatistics, Statistics, or related field
Fluency in Mandarin
Experience with statistical programming such as SAS, R, Python
Experience with CDISC and CDASH standards
Strong knowledge and experience in clinical trial design and data analysis, with ability to communicate statistical concepts
Strong knowledge in applied statistics and data analysis methodology including regression modeling, categorical data analysis, survival analysis, etc.
Strong knowledge of clinical research, drug development process, and medical terminology; oncology experience preferred
Excellent oral and written communication skills
Excellent presentation skills
Salary The expected base salary range for this position is $80,000 – $140,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills. While most offers typically fall within the low to mid‑point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise align strongly with the requirements of the role.
Benefits
100% paid employee premiums for medical, dental, and vision coverage
Short‑term and long‑term disability insurance
401(k) plan with a 50% company match of up to 3% (with a vesting schedule of 5 years)
15 paid time off days per year, sick leave, plus 11 paid holidays
Additional benefits included (details upon offer)
Equal Opportunity Employer SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
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Location This position requires a full‑time onsite presence at our Redmond, WA office location. Working some evenings may be required for collaboration and meetings with teams in China.
Responsibilities
Provide data‑driven insights and statistical support to clinical teams, offering guidance on data‑related challenges and participating in project team meetings as needed
Collaborate with clinical teams on study design and clinical study protocol development
Develop, validate, and maintain programs (e.g., SAS program) and conduct comprehensive data analysis using SAS, R, or other statistical software to generate TLFs as needed
Conduct and interpret interim analysis, including statistical and pharmacokinetics analysis, to support clinical decision making
Develop and review SAP, including table/listing/figure shells, and review final SAR and CSR
Oversee and validate CRO programming activities, ensuring accuracy in internally or externally produced SDTM, ADaM, SAS tables, listings, and figures
Conduct quality control of project deliverables, ensuring compliance with data integrity and reporting standards
Perform simulations and ad‑hoc statistical analysis when needed
Understand and apply regulatory guidelines and industry standards practices on statistics and SAS programming
Qualifications
Master’s Degree with 3+ years of statistical work experience or PhD in Biostatistics, Statistics, or related field
Fluency in Mandarin
Experience with statistical programming such as SAS, R, Python
Experience with CDISC and CDASH standards
Strong knowledge and experience in clinical trial design and data analysis, with ability to communicate statistical concepts
Strong knowledge in applied statistics and data analysis methodology including regression modeling, categorical data analysis, survival analysis, etc.
Strong knowledge of clinical research, drug development process, and medical terminology; oncology experience preferred
Excellent oral and written communication skills
Excellent presentation skills
Salary The expected base salary range for this position is $80,000 – $140,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills. While most offers typically fall within the low to mid‑point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise align strongly with the requirements of the role.
Benefits
100% paid employee premiums for medical, dental, and vision coverage
Short‑term and long‑term disability insurance
401(k) plan with a 50% company match of up to 3% (with a vesting schedule of 5 years)
15 paid time off days per year, sick leave, plus 11 paid holidays
Additional benefits included (details upon offer)
Equal Opportunity Employer SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
#J-18808-Ljbffr