ABOUT 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
We are seeking a Director of Clinical Biomarkers to lead the biomarker strategy and execution across our autoimmune clinical pipeline. This is a scientifically rich cross-functional role sitting at the intersection of translational biology, clinical development, and precision medicine. You will help to define how we measure target and pathway engagement, pharmacodynamic response, and disease modification across our programs — and you will translate those insights into regulatory-grade evidence that supports our clinical and commercial strategies You will partner closely with other functions to integrate biomarker data into clinical programs and advance development, and you will have the opportunity to establish the Biomarker function as a core pillar of our development organization.
What You'll Do
Define and lead the end-to-end biomarker strategy for one or more autoimmune pipeline programs, encompassing pharmacodynamic, predictive, prognostic, and safety biomarkers
Develop and execute biomarker plans integrated into clinical protocols, including sample collection strategies, assay selection, and analytical frameworks
Partner with other functions to translate preclinical mechanistic findings into clinical biomarker hypotheses and early proof-of-mechanism readouts
Oversee biomarker assay development, validation, and implementation in collaboration with internal and external laboratory partners, ensuring fit-for-purpose analytical performance
Lead analysis and interpretation of clinical biomarker data, enabling team discussion and decision-making around dose selection, patient enrichment, and go/no-go decisions
Develop biomarker analysis plans and ensure analytical rigor for biomarker endpoints
Author biomarker-related sections of clinical protocols, SAPs, clinical study reports, IND/IMPD submissions, and regulatory briefing documents
Support health authority interactions on biomarker strategy and companion diagnostic (CDx) development pathways where applicable
Evaluate emerging biomarker technologies and platforms relevant to immunology and inflammation, and recommend adoption where scientifically and operationally justified
Assist with management of CRO and specialty laboratory partnerships for biomarker sample processing, analysis, and data delivery
Help build a biomarker function that is scientifically rigorous, operationally excellent, and strategically aligned with program needs