Clinical Research Biostatistician
80K–140K a year
Behavioral Health Market Context
Apply Nowvia Jooble
Benefits
Health InsurancePaid Time OffDental Coverage
Job Description
al cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. The biostatistician will collaborate with the senior level biostatisticians on clinical or non-clinical studies. The successful candidate for this position will leverage data science and statistics expertise to support the data cleaning, visualization, analysis, and reporting for new drug discovery efforts.
This position requires a full-time onsite presence at our Redmond, WA office location.
Provide data-driven insights and statistical support to clinical teams, offering guidance on data-related challenges and participating in project team meetings as needed.
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.
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.
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.
This position will require working some evenings due to collaboration and meetings with our teams in China.
SystImmune is a leading and well-funded biotech company with a bright future. 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 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, plus 11 paid holidays and MORE.
This position requires a full-time onsite presence at our Redmond, WA office location.
Provide data-driven insights and statistical support to clinical teams, offering guidance on data-related challenges and participating in project team meetings as needed.
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.
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.
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.
This position will require working some evenings due to collaboration and meetings with our teams in China.
SystImmune is a leading and well-funded biotech company with a bright future. 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 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, plus 11 paid holidays and MORE.
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
- •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
- •This position will require working some evenings due to collaboration and meetings with our teams in China
Benefits
- •100% paid employee premiums for medical/dental/vision, also STD, LTD, a 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, plus 11 paid holidays and MORE
Responsibilities
- •The biostatistician will collaborate with the senior level biostatisticians on clinical or non-clinical studies
- •The successful candidate for this position will leverage data science and statistics expertise to support the data cleaning, visualization, analysis, and reporting for new drug discovery efforts
- •This position requires a full-time onsite presence at our Redmond, WA office location
- •Provide data-driven insights and statistical support to clinical teams, offering guidance on data-related challenges and participating in project team meetings as needed
- •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
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