Biostatistician - Bilingual Mandarin

Oncology
$80K - $140K/yr(estimated)

Description

<p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">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 bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has 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 discover 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.</span></span></p><p><span style="font-size:14px;">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.</span><br>&#160;</p><p><span style="font-size:14px;">This position requires a full-time onsite presence at our Redmond, WA office location.</span><br>&#160;</p><p><span style="font-size:14px;"><strong>Responsibilities:</strong></span></p><ul><li><span style="font-size:14px;">Provide data-driven insights and statistical support to clinical teams, offering guidance on data-related challenges and participating in project team meetings as needed.</span></li><li><span style="font-size:14px;">Collaborate with clinical teams on study design and clinical study protocols development.</span></li><li><span style="font-size:14px;">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.</span></li><li><span style="font-size:14px;">Conduct and interpret interim analysis, including statistical and pharmacokinetics analysis, to support clinical decision making.</span></li><li><span style="font-size:14px;">Develop and review SAP, including table/listing/figure shells, and review final SAR and CSR.</span></li><li><span style="font-size:14px;">Oversee and validate CRO programming activities, ensuring accuracy in internally or externally produced SDTM, ADaM, SAS tables, listings, and figures.</span></li><li><span style="font-size:14px;">Conducts quality control of project deliverables, ensuring compliance with data integrity and reporting standards.</span></li><li><span style="font-size:14px;">Perform simulations and ad-hoc statistical analysis when needed.</span></li><li><span style="font-size:14px;">Understand and apply regulatory guidelines and industry standards practices on statistics and SAS programming.</span></li></ul><p><span style="font-size:14px;"><strong>Qualifications:</strong></span></p><ul><li><span style="font-size:14px;">Master&#8217;s Degree with&#160;3+ years of statistical work experience&#160;or PhD&#160;in Biostatistics, Statistics, or related field.</span></li><li><span style="font-size:14px;">Fluency in Mandarin.</span></li><li><span style="font-size:14px;">Experience with statistical programming such as SAS, R, Python.</span></li><li><span style="font-size:14px;">Experience with CDISC and CDASH standards.</span></li><li><span style="font-size:14px;">Strong knowledge and experience in clinical trial design and data analysis, with ability to communicate statistical concepts.</span></li><li><span style="font-size:14px;">Strong knowledge in applied statistics and data analysis methodology including regression modeling, categorical data analysis, survival analysis, etc.</span></li><li><span style="font-size:14px;">Strong knowledge of clinical research, drug development process, and medical terminology, and oncology experience preferred.</span></li><li><span style="font-size:14px;">Excellent oral and written communication skills.</span></li><li><span style="font-size:14px;">Excellent presentation skills.</span></li></ul><span style="font-size:14px;"><strong>This position will require working some evenings due to collaboration and meetings with our teams in China.</strong><br><br>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&#8217;s qualifications, experience, and skills.<br>While most offers typically fall within the <span style="font-weight:bold;">low to mid-point of the range</span>, we may extend an offer toward the <span style="font-weight:bold;">higher end</span> for exceptional candidates whose background and expertise <strong>exceeds</strong> the requirements of the role.</span><br><br><strong>SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company&#8217;s success. SystImmune offers a comprehensive benefits package including: 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.</strong><p><strong>We offer an opportunity for you to learn and grow while making significant contributions to the company&#8217;s success.&#160;</strong></p><p><strong>SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.</strong></p>
SystImmune

SystImmune

BIOTECHNOLOGY

Novel therapeutic bi-specific, and multi-specific antibodies, antibody-drug conjugates

LocationWA - Redmond
Open Jobs47
OncologyNeurology
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