Biostatistician - Bilingual Mandarin

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ, specializing in developing innovative cancer treatments using its established drug development platforms. The company focuses on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs), with multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery and IND-enabling stages, representing cutting-edge biologics development.

About the role

The biostatistician will collaborate with senior-level biostatisticians on clinical or non-clinical studies, leveraging data science and statistics expertise to support data cleaning, visualization, analysis, and reporting for new drug discovery efforts. This position requires a full-time onsite presence at our Bothell, WA office location starting September 2026.

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 protocols development
• Develop, validate, and maintain programs (e.g., SAS programs) 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

Requirements

• 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

Schedule

This position will require working some evenings due to collaboration and meetings with teams in China.

Pay

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 exceed the requirements of the role.

Benefits

• 100% paid employee premiums for medical, dental, and vision
• Short-term and long-term disability coverage
• 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years
• 15 PTO days per year
• Sick leave
• 11 paid holidays