Scientist/Senior Scientist, Clinical Pathology & IHC
SystImmune
2h ago
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> <br>We are seeking 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). </span></span><p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">This role requires strong expertise 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. </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. </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. <br><br><strong>Key Responsibilities </strong></span></span></p><p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">IHC Assay Development & Validation </span></span></p><ul><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Develop and optimize IHC assays on FFPE tissues for biomarker and CDx applications </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 GxP environments </span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Perform antibody selection, titration, and qualification </span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Support multiplex IHC/IF development </span></span></li></ul><p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Biomarker Strategy & Clinical Integration </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) </span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Support CDx development and clinical implementation </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 </span></span></li></ul><p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Data Analysis & Interpretation </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 </span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Collaborate on scoring algorithms and cutoff development </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 </span></span></li></ul><p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Documentation, Compliance & Collaboration </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 GxP </span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Support audits and inspections </span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Collaborate with internal teams and external partners </span></span></li></ul> <p><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;"><strong>Qualifications </strong></span></span></p><ul><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">PhD with 2–5+ 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 </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 </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 </span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Demonstrated experience in oncology biomarker development </span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Experience working in regulated environments (CLIA/CAP, GxP) </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 </span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Expertise with GraphPad, ROC analysis, and biomarker cutoff determination. 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 in automated IHC platforms (Ventana, Leica, or equivalent) </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 </span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Familiarity with translational biomarker strategies </span></span></li><li><span style="font-size:14px;"><span style="font-family:Arial, Helvetica, sans-serif;">Excellent documentation and quality compliance practices </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’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;"> </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’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;"> </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’s success. </span></span></span><br><span style="font-size:8.25pt;"><span style="font-family:Arial;"> </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> 
SystImmune
BIOTECHNOLOGY
Novel therapeutic bi-specific, and multi-specific antibodies, antibody-drug conjugates
LocationWA - Redmond
Open Jobs49
OncologyNeurology
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