What are the responsibilities and job description for the Scientist I/II, Clinical Biomarkers position at Nurix Therapeutics?
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix’s dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch disease.
The Position
The successful candidate will be responsible for the execution of translational activities toward Nurix’s clinical development programs targeting protein fate for cancer targeted therapy and immunotherapy. Collaborating with the multiple organizations at Nurix, the translational Sci I / II will be responsible for executing preclinical studies, analysis, and interpretation of data to guide indication selection for early clinical development.
Specific responsibilities include :
- Utilize broad technical expertise in cell and tumor immunology, biochemistry, and molecular biology to investigate, develop and optimize new methods to expand mechanistic understanding of Nurix’s clinical development assets.
- Build and maintain a knowledge of current and emerging biomarker assay technologies in area of expertise.
- Incorporate state of the art technological advances into biomarker and clinical strategies to guide indication selection, and combination strategies for global development
- Oversight of technical transfer of clinical biomarker assays to partner labs
- Responsible for the biomarker strategy for clinical studies; working closely with the clinical team and non-clinical stakeholders
- Support scientific input and review of all translational medicine aspects of clinical and regulatory documents, including but not limited to development plans, study protocols, clinical study reports and regulatory submissions.
- Communicate translational research efforts to collaborators, corporate partners, and / or at scientific meetings
Education and Skills Requirements :
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