Associate Director, Clinical Supply
ConfidentialABOUT LAKEFRONT BIOTHERAPEUTICS Lakefront Biotherapeutics is a global biotech with offices in Belgium, Chicago and San Francisco, focused on building a differentiated immunology and inflammation pipeline to address serious diseases with high unmet medical need. Our pipeline is anchored by T‑cell engager programs, led by a potential first‑in‑class clinical asset and complemented by an exciting preclinical portfolio in autoimmune disease. Our lead asset is being developed for severe immune‑mediated diseases, while additional preclinical programs expand the long‑term potential of our R&D pipeline. At Lakefront, we focus on advancing programs with strong biological rationale, clear clinical proof of concept and large commercial opportunities. Are you ready to transform lives and be part of a journey like no other? We are building a company where science, execution, and accountability matter. Rather than layers of hierarchy, we operate with small, empowered teams that work hands‑on across development stages to move programs forward efficiently and thoughtfully. We are looking for people who want to contribute directly, who are motivated by solving real problems, collaborating across disciplines, and taking ownership from idea to impact. At Lakefront, every role plays a part in shaping the future of medicines that have the potential to make a meaningful difference for patients. If you are driven to improve the lives of patients, energized by execution, and excited to help build a growing company with a strong balance sheet, we look forward to meeting you. The Role Lakefront Biotherapeutics is seeking an Associate Director of Clinical Supply Chain to plan and deliver investigational product for its clinical studies. The Associate Director will own clinical supply strategy from demand forecasting through packaging, labeling, distribution, inventory management, and reconciliation. The role will work closely with Clinical Operations, Technical Operations, Quality, Regulatory Affairs, and external vendors to keep studies supplied as enrollment and timelines change. This role is hybrid and the successful candidate must be able to work onsite in our South San Francisco office 2-3 days/week. What You'll Do Develop clinical supply plans and forecasts based on study design, enrollment projections, dosing schedules, site activation, and expiry dating. Manage supply requirements for study startup, ongoing enrollment, protocol amendments, and closeout. Oversee external partners responsible for packaging, labeling, storage, distribution, and returns or destruction of clinical trial material. Develop and review packaging and labeling plans for global studies in collaboration with Quality and Regulatory Affairs, ensuring alignment with applicable ICH guidelines and country-specific requirements. Establish inventory targets, monitor stock at depots and clinical sites, and coordinate resupply to reduce the risk of shortages or waste. Coordinate international shipments, import requirements, and country-specific labeling with internal teams and qualified partners. Manage temperature-controlled storage and transportation, including excursion assessment with Quality and Technical Operations. Support the setup and ongoing management of clinical supply functions in interactive response technology (IRT) systems, as applicable. Maintain accurate supply records, forecasts, budgets, vendor timelines, and performance measures. Identify supply risks early and lead contingency planning for changes in enrollment, manufacturing schedules, or study scope. Partner with Quality to ensure activities comply with applicable GxP requirements, approved procedures, and clinical trial documentation standards. What You Bring Bachelor's degree in supply chain, life sciences, business, or a related field; advanced degree preferred. Typically 8 or more years of experience in pharmaceutical or biotechnology supply chain, including substantial experience supporting clinical trials…