Teams at N-Power Medicine

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.

Lead day-to-day operations and performance of Clinical Research Specialist teams across assigned health system accounts. Manage hiring, onboarding, training, coaching, compliance, quality oversight, and site relationships. Track performance metrics, support audits and corrective actions, and implement process improvements while partnering with senior leadership to ensure operational excellence and alignment with account priorities.

Provide Tier 1/2 remote IT support, manage corporate IT systems and applications, onboard/offboard employees, patch and maintain laptops via Iru MDM, enforce security controls (MFA/SSO), handle Zoom A/V issues, maintain inventory, and use Jira for ticketing and tracking.