Staff, Product Development Lifecycle

About N-Power Medicine
N-Power Medicine aims to establish a new paradigm in drug development by reinventing the ‘how’ and transforming clinical trials through better integration with clinical practice, ensuring broader participation by physicians and patients. We are building an exceptional multi-disciplinary team with diverse expertise spanning healthcare, engineering, technology and regulatory, and with people who share our core value of Empowering Community through generosity, curiosity and humility. We are working with urgency to bring better therapies to patients faster.
Position Overview
N-Power Medicine is hiring a Staff, Product Development Lifecycle, Release & Quality to join their team reporting to the Senior Director, Product Management. This individual will serve as the critical liaison between healthcare product management, operations, oncology data, and engineering - translating product requirements into engineering delivery, holding engineering accountable to the product roadmap, and ensuring that everything shipped meets the quality bar for a clinical-facing product. This role owns the health of the product development lifecycle: how requirements move into build, how releases are planned and validated, how experimentation (A/B testing) is designed and read out, and how quality is verified before anything reaches physicians, patients, or clinical operations teams.
Success depends on the individual’s ability to work cross-functionally and hold engineering, product, and clinical operations partners accountable to committed deliverables without formal authority over them.
*This is a hybrid on-site role, Bay Area is preferred.
Role Objectives and Responsibilities
Serve as the primary liaison between oncology product management, clinical research operations, analytics teams, and engineering - ensuring requirements are clearly understood, scoped, and correctly implemented; build credibility and bridge communication across disciplines
Translate product re...