Biostatistician - Bilingual Mandarin

Systimmune•Bothell, WA

4d•$80,000 - $140,000•Onsite

About The Position

SystImmune is seeking a Biostatistician to collaborate with senior biostatisticians on clinical or non-clinical studies. The successful candidate will leverage data science and statistics expertise to support data cleaning, visualization, analysis, and reporting for new drug discovery efforts. This is a full-time, onsite position requiring presence at our Bothell, WA office. The role involves providing data-driven insights and statistical support to clinical teams, participating in project team meetings, and collaborating on study design and protocol development. The biostatistician will also be responsible for developing, validating, and maintaining statistical programs (e.g., SAS), conducting comprehensive data analysis using SAS, R, or other statistical software, and generating TLFs. This includes performing interim analyses, developing and reviewing SAPs, overseeing CRO programming activities, conducting quality control of project deliverables, performing simulations, and applying regulatory guidelines. Fluency in Mandarin is required, and some evening work may be necessary for collaboration with teams in China.

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, and oncology experience preferred.
Excellent oral and written communication skills.
Excellent presentation skills.

Nice To Haves

Oncology experience preferred.

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 (eg. 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.
Conducts 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.