Oncology Clinical Development Scientist

<span style="font-size:10.5pt;"><span style="font-family:Arial;">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><br><br><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;"><span style="line-height:115%;">As an Oncology Strategy Lead supporting oncology clinical development, you will serve as the scientific and strategic right-hand to the clinical development leader.&#160; Your mission is to support critical elements of oncology clinical development programs in project management, competitive intelligence, and data insights generation.</span><br><br><span style="line-height:115%;"><strong>Key Responsibilities</strong></span></span></span><div style="margin-left:8px;"><ul style="margin-bottom:11px;"><li style="margin-left:8px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;"><span style="line-height:115%;"><b>Landscape Surveillance:</b> Monitor and analyze clinical trial readouts, regulatory filings (FDA/EMA), and patent landscapes for key competitors in the relevant space.</span></span></span></li><li style="margin-left:8px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;"><span style="line-height:115%;"><b>Strategic Benchmarking:</b> Compare internal clinical protocols against competitor trials to identify "Best-in-Class" opportunities. Advise teams on endpoint selection (e.g., mPFS vs. ORR) and patient stratification strategies.</span></span></span></li><li style="margin-left:8px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;"><span style="line-height:115%;"><b>Medical Congress Leadership:</b> Lead the intelligence gathering at major conferences (ASCO, ESMO, WCLC and ASH). Coordinate onsite intelligence gathering and rapidly synthesize findings for executive leadership.</span></span></span></li><li style="margin-left:8px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;"><span style="line-height:115%;">T<b>arget Product Profile (TPP) Development:</b> Collaborate with Commercial and R&amp;D teams to define the TPP of our pipeline assets to ensure they are competitive at the time of launch.</span></span></span></li><li style="margin-bottom:11px;margin-left:8px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;"><span style="line-height:115%;"><b>Ad-hoc Analysis: </b>Provide rapid response "Deep Dives" on evolving competitive landscape and key data readout.</span></span></span></li><li style="margin-bottom:11px;margin-left:8px;"><span style="font-family:Arial, Helvetica, sans-serif;"><span style="font-size:14px;"><b><span style="line-height:115%;">Project Management:</span></b><span style="line-height:115%;"> support the Clinical Development Leader in cross-functional meetings, track trial progress timeline, and flag risk areas and opportunities.</span></span></span></li></ul>