Drug Safety Physician

Title: Drug Safety PhysicianNurix 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.PositionAs a Drug Safety Physician, you will play a key role in ensuring the safety of patients in Nurix’s clinical trials. You will apply your clinical expertise to evaluate safety data, guide benefit–risk assessments and help shape the pharmacovigilance strategy for Nurix’s emerging therapies. You will report to the VP of pharmacovigilance and work closely with colleagues in clinicaldevelopment, regulatory affairs, and clinical research to interpret emerging safety signals, support regulatory submissions, and maintain a strong safety framework during clinical development and transition into the post-marketing phase. Your insights will help inform critical decisions about patient safety, risk management, and the overall development strategy for our products. This role is well suited for a physician who enjoys working at the intersection of non-clinical data, clinical medicine, data interpretation, and drug development, and who wants to have a meaningful impact on how new therapies are evaluated and brought to patients.ResponsibilitiesMedical Safety Leadership Serve as the medical safety lead for assigned products, providing clinical and pharmacovigilance expertise to safety strategy and activities.Lead aggregate safety data analysis for signal detection, signal evaluation, and risk characterization.Conduct medical review and interpretation of safety data, contributing to benefit–risk assessments.Monitor emerging safety signals and proactively address potential safety risks through appropriate internal and external communication.Regulatory and Safety Documentation Contribute to safety responses to regulatory authorities and participate in regulatory interactions.Provide clinical leadership during inspections and audits related to safety and risk management.Author and review regulatory safety documents, including:DSURsSafety sections of INDs, and regulatory briefing books.Clinical Development Support Provide clinical input into safety aspects of clinical trial protocols, informed consent forms, and investigator brochures.Collaborate with clinical development, regulatory affairs, medical affairs, and other stakeholders to ensure a consistent global safety strategy.Governance and Cross-Functional CollaborationServe on safety governance committees, supporting strategic decision-making for risk mitigation and benefit–risk evaluationRequirementsMedical degree is requiredClinical experience preferred10+ years of experience in pharmacovigilance/ drug safety within the pharmaceutical or biotechnology industryDemonstrated expertise in aggregate safety analysis and benefit–risk evaluationStrong knowledge of global pharmacovigilance regulations and guidance (ICH, FDA, EMA, MHRA)Experience supporting early and late-stage clinical development, regulatory submissions, and product launchExperience in post-marketing safety surveillance and risk managementExperience interacting with global health authorities on safety mattersFamiliarity with signal detection and safety surveillance tools and databasesStrong communication, collaboration, and cross-functional leadership skillsAbility to interpret complex clinical and safety data and translate insights into regulatory and business strategyAbility to work effectively and collaboratively in a fast-paced, growing organizationFit with Nurix Culture and ValuesStrong team orientation; highly collaborativeSolutions and results-oriented focusHands-on approach; resourceful and open to diverse points of viewSalary Range: 307K - 351K plus bonus & equityApplication ProcessNurix is an Equal Opportunity Employer offering a competitive salary and benefits package. Applicants should be legally entitled to work for any employer in the US.Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy (https://www.nurixtx.com/privacy-policy/).