Careers - Maze TherapeuticsMaze on LinkedinMaze on Linkedin

You'll **lead biostatistical strategy** across clinical studies at a **clinical-stage biopharmaceutical company**. You'll drive study design, regulatory submissions, and CRO oversight, blending hands-on analysis with strategic leadership.

You'll build and lead the safety science and pharmacovigilance function at a **clinical-stage biopharmaceutical company**. You'll shape safety strategy across nephrology and cardiometabolic programs, ensuring patient safety remains central to all development decisions. This is a highly visible, hands-on leadership role reporting to the Head of Clinical Development.

You'll provide **regulatory leadership** for clinical-stage programs at a biopharmaceutical company. Your core impact will be ensuring **successful regulatory submissions and Health Authority interactions**. This role offers the chance to shape regulatory strategy in a **fast-paced precision medicine environment**.

You'll lead clinical development for a **SLC6A19 program** targeting chronic kidney disease and PKU at **Maze Therapeutics**, translating genetic insights into life-saving medicines. Your work will drive early-stage clinical trials from first-in-human to proof-of-concept, collaborating with cross-functional teams.

You'll design and scale production-grade ML infrastructure for drug discovery at a clinical-stage biopharmaceutical company. You'll build data pipelines and deploy models that directly impact **drug development programs** and enable **data-driven scientific decision-making**.

You'll shape the data foundation of clinical development programs, collaborating with Biostatistics, Clinical Data Management, Clinical Operations, and Regulatory Affairs. You'll lead **statistical programming strategy** and execution across multiple studies, ensuring **regulatory-compliant outputs** that drive smarter decisions. This role offers the chance to **automate workflows** and manage external vendors in a hybrid work environment.

You'll co-lead **Phase 2 CKD clinical trials** from protocol development to study close-out. You'll manage external vendors and CROs, ensuring **adherence to ICH GCP guidelines**. This role offers hands-on impact in a precision medicine biotech.