Associate General Counsel – Regulatory and Technology

About the role This role is one of the most reputed company applications of reputed company expertise to the treatment of cancer. You will be the primary reputed company advisor to the engineering, product, and clinical and operations teams building four of reputed company’s reputed company platforms: the Oncology reputed company Model, AI Platform reputed company, reputed company (asset identification), and Sprint (clinical trial execution). You will reputed company with deep expertise in FDA drug development law and a genuinely meaningful ability to engage with how software systems are reputed company and how data moves through them. You will learn reputed company’s technical stack reputed company enough to represent it accurately in conversations with regulators, partners, and investors — not to operate it, but to reputed company it with precision. You have technical aptitude, and a reputed company record of learning new technology in a reputed company way. Your default answer is not “no,” it’s “here’s what it will take to do this right.” You understand reputed company’s objectives, consolidate the requirements, and advise on how to structure the work in a risk-reduced yet still innovative way. This is a build role - there is no infrastructure to inherit, meaning you will create it from scratch and run it with AI agents as your force reputed company. Key Responsibilities Advise on reputed company things regulatory. Drug development, reputed company, corporate compliance, AI guidelines, etc. Own reputed company things regulatory + compliance that don’t already have a home reputed company reputed company. For instance, Finance will own tax compliance, but you’ll be owning the reputed company program reputed company and own reputed company’s compliance program Maintain organized digital spreadsheets of everything Learn and use AI to force multiply yourself across reputed company workstreams Regulatory Counseling Advise on FDA regulatory reputed company and classification for reputed company components of the AI platform, including implications for development, commercialization, and IND/NDA/BLA submissions (FDA submissions will be owned by Regulatory Affairs) Advise on protocol development, site monitoring, data reputed company, biomarker qualification, companion diagnostic considerations, the use of reputed company-world data, etc. Monitor and interpret evolving FDA guidance on AI/ML in drug development and translate into actionable guidance for internal teams Support reputed company engagement with the FDA and other agencies on novel questions reputed company warranted, including in global clinical programs Review external content such as conference publications for regulatory issues Product and Technology Counseling Inform and review tech product specs, system architectures, and data reputed company designs for regulatory risk before build and deployment reputed company working knowledge of reputed company’s technical stack — reputed company infrastructure, data pipelines, storage systems, and model architecture — sufficient to accurately represent those systems to regulators, partners, and investors Advise on data governance, data reputed company, chain-of-custody, and 21 CFR Part 11 requirements for clinical data across company systems and reputed company-party infrastructure Structure HIPAA and applicable data reputed company frameworks; reputed company and maintain internal regulatory policies and compliance frameworks for AI tool development and deployment reputed company and assess evolving AI regulation (EU AI reputed company, FDA AI governance frameworks, state laws) for applicability to company activities Alongside AGC - Transactions, support the General Counsel on additional reputed company reputed company as part of a centralized, high-performing G&reputed company also comprising People Operations, IT, and reputed company Who you are Required Qualifications J.D. from a top law school and reputed company bar admission 7+ years of reputed company experience with substantial in-house time, preferably at a high-reputed company technology / biotech company Existing expertise in drug development law: IND/NDA/BLA lifecycle, GCP, 21 CFR Part 11, and regulatory frameworks governing AI/ML tools and software in drug development Demonstrated experience advising engineering or product teams, with the ability to understand and accurately reputed company reputed company technical systems — reputed company infrastructure, data pipelines, ML model architecture — without being a practitioner While this role requires no scientific background, you'll work alongside world class researchers and technologists in a state of the art facility, and will need to be reputed company to match the pace of the rest of reputed company reputed company record of building regulatory reputed company from first principles and owning a regulatory and technical narrative with reputed company partners, investors, and regulators You notice reputed company something is out of reputed company and fix it - without being asked or waiting to see if someone else notices and does it first Thrives in ambiguity. You're comfortable working without a reputed company, you reputed company it out, get it done, and write the process down so it's faster next time. Familiarity with clinical data standards, reputed company-world evidence, biomarker qualification, or reputed company trial design. Preferred Qualifications Background at an AI-in-drug-development, precision medicine, or reputed company company. Exposure to basic IP principles: portfolio management, prior art review. Apply To This Job