Senior Scientist, Discovery Biology
Newark, CA (On-site)
Discovery Biology
Protagonist Therapeutics is a clinical-stage biopharmaceutical company pioneering a new generation of peptide-based therapeutics to address unmet needs in immunology, metabolic diseases, and hematology. We leverage a powerful peptide discovery platform to design highly selective and orally delivered agents targeting validated pathways. Our Discovery Biology team plays a central role in advancing innovative molecules from concept to clinic.
We are seeking a highly motivated and scientifically rigorous Senior Scientist to join our Discovery Biology team reporting to Sr Director, Biology. The ideal candidate will have deep expertise in immunology and inflammation, and a proven ability to drive experimental research from concept to data-driven insight. This is a hands-on lab-based role with opportunities to lead key discovery-stage projects and contribute strategically to pipeline advancement.
The base pay range for this position at commencement of employment is expected to be between $150K and $175K / year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.
Protagonist Therapeutics is a discovery through late-stage development biopharmaceutical company. Two novel peptides, icotrokinra and rusfertide, derived from Protagonist's proprietary discovery platform are currently in advanced Phase 3 clinical development, with New Drug Application submissions to the FDA expected in 2025. Icotrokinra (JNJ-2113) is a first-in-class investigational targeted oral peptide that selectively blocks the Interleukin-23 receptor ("IL-23R") which is licensed to Janssen Biotech, Inc., a Johnson & Johnson company. Following icotrokinra's joint discovery by Protagonist and Johnson & Johnson scientists pursuant to the companies' IL-23R collaboration, Protagonist was primarily responsible for development of icotrokinra through Phase 1, with Johnson & Johnson assuming responsibility for development in Phase 2 and beyond. Rusfertide, a mimetic of the natural hormone hepcidin, is currently in Phase 3 development for the rare blood disorder polycythemia vera (PV). Rusfertide is being co-developed and will be co-commercialized with Takeda Pharmaceuticals pursuant to a worldwide collaboration and license agreement entered into in 2024 under which the Company remains primarily responsible for development through NDA filing. The Company also has a number of pre-clinical stage oral drug discovery programs addressing clinically and commercially validated targets, including the IL-17 oral peptide antagonist PN-881, an oral hepcidin program, and an oral obesity program.