Teams at N-Power Medicine

Lead Quantitative Sciences for oncology clinical development, designing and executing externally controlled and hybrid studies. Develop statistical methodologies for bias mitigation, design protocols and analysis plans, implement analyses and scalable tools, mentor teams, collaborate cross-functionally on data requirements, and communicate results via publications and regulatory reports.

Senior account and implementation leader managing end-to-end partnership operations with oncology network partners. Owns partner activation, physician engagement, EHR integration, implementation, ongoing program performance, and scaling repeatable playbooks while coordinating cross-functionally and supporting BD at contract handoff.

Lead day-to-day execution and continuous improvement of the Quality Management System and clinical trial quality oversight. Administer and optimize the electronic QMS, manage CAPA, audits, document control, vendor management, and SDLC compliance for regulated software. Mentor a small quality team, partner cross-functionally with clinical and engineering teams, and ensure regulatory compliance with GCP, 21 CFR Part 11, ISO 9001 and FDA requirements.