Scientist/Senior Scientist, Clinical Pathology & IHC

SeniorOncologyADCs (Antibody-Drug Conjugates)
$90K - $140K/yr(estimated)

Description

<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.<br>&#160;<br>We are&#160;seeking&#160;a highly motivated Scientist / Senior Scientist to lead and support the development, optimization, and validation of immunohistochemistry (IHC) and tissue-based biomarker assays for clinical and translational research programs, including companion diagnostics (CDx).&#160;</span></span><p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">This role requires strong&#160;expertise&#160;in histology, IHC, and oncology biomarker development, along with the ability to design experiments, interpret complex data, and drive translational strategies from preclinical to clinical stages. The successful candidate will work cross-functionally with pathologists, translational scientists, clinical teams, and external partners to enable biomarker-driven clinical trials, particularly in antibody-drug conjugate (ADC) programs.&#160;</span></span></p><p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">The ideal candidate will have experience bridging preclinical biology, translational science, and clinical biomarker implementation, including support for global regulatory strategies (FDA/NMPA) and CDx co-development.&#160;</span></span></p><p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">This position is full-time onsite at our Redmond, WA location.&#160;<br><br><strong>Key Responsibilities&#160;</strong></span></span></p><p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">IHC Assay Development &amp; Validation&#160;</span></span></p><ul><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Develop and&#160;optimize&#160;IHC assays on FFPE tissues for biomarker and CDx applications&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Support validation studies in CLIA/CAP and/or&#160;GxP&#160;environments&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Perform antibody&#160;selection, titration, and qualification&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Support multiplex IHC/IF development&#160;</span></span></li></ul><p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Biomarker Strategy &amp; Clinical Integration&#160;</span></span></p><ul><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Contribute to biomarker strategies (e.g., PD-L1, HER2)&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Support CDx development and clinical implementation&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Ensure alignment with FDA and NMPA regulatory requirements&#160;</span></span></li></ul><p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Data Analysis &amp; Interpretation&#160;</span></span></p><ul><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Analyze and interpret IHC results and digital pathology data&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Collaborate on scoring algorithms and cutoff development&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Present findings and support scientific and regulatory reporting&#160;</span></span></li></ul><p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Documentation, Compliance &amp; Collaboration&#160;</span></span></p><ul><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Author SOPs and ensure compliance with CLIA, CAP, and&#160;GxP&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Support audits and inspections&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Collaborate with internal teams and external partners&#160;</span></span></li></ul>&#160;<p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><strong>Qualifications&#160;</strong></span></span></p><ul><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">PhD with 2&#8211;5+ years of experience in biotech, life science, biopharma</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Strong experience with GraphPad, ROC analysis, and biomarker cutoff determination&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Strong experience in IHC assay development, optimization, and validation&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Experience supporting clinical trials, translational research, and/or CDx development&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Demonstrated&#160;experience in oncology biomarker development&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Experience working in regulated environments (CLIA/CAP,&#160;GxP)&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Ability to lead projects and collaborate across multidisciplinary teams&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Expertise&#160;with GraphPad, ROC analysis, and biomarker cutoff determination.&#160;Strong data analysis, interpretation, and scientific communication skills </span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Expertise&#160;in automated IHC platforms (Ventana, Leica, or equivalent)&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Strong understanding of antibody biology, tumor biology, and tissue-based assays&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Familiarity with translational biomarker strategies&#160;</span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Excellent documentation and quality compliance practices&#160;</span></span></li></ul><br><span style="font-size:10.5pt;"><span style="font-family:Arial;"><span style="font-weight:bold;">Compensation and Benefits:</span></span></span><br><span style="font-size:10.5pt;"><span style="font-family:Arial;">The expected base salary range for this position is $90,000 - $140,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate&#8217;s level, qualifications, experience, and skills.</span></span><br><span style="font-size:10.5pt;"><span style="font-family:Arial;">While most offers typically fall within the <span style="font-weight:bold;">low to mid-point</span> of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.</span></span><br><span style="font-size:11pt;"><span style="font-family:Arial;">&#160;</span></span><br><span style="font-size:8.25pt;"><span style="font-family:Arial;"><span style="font-weight:bold;">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.</span></span></span><br><span style="font-size:8.25pt;"><span style="font-family:Arial;">&#160;</span></span><br><span style="font-size:8.25pt;"><span style="font-family:Arial;"><span style="font-weight:bold;">We offer an opportunity for you to learn and grow while making significant contributions to the company&#8217;s success. </span></span></span><br><span style="font-size:8.25pt;"><span style="font-family:Arial;">&#160;</span></span><br><span style="font-size:8.25pt;"><span style="font-family:Arial;"><span style="font-weight:bold;">SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.</span></span></span><br>&#160;
SystImmune

SystImmune

BIOTECHNOLOGY

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

LocationWA - Redmond
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OncologyNeurology
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