RDI
Clinical Monitoring Standards Lead
Los Angeles, California, United States
Sponsorship not specifiedDetected 31 days ago
Leadership
About the role
- We have a passionate, caring, hard-working clinical operations team that wants to perfect its craft.
- We are looking for someone who can raise the standard across the team and make sure that standard holds across every study.
- You will also help modernize clinical trial monitoring as the industry moves toward risk-based monitoring, real-time oversight, remote-first execution, and AI-assisted workflows without compromising quality.
Responsibilities
- The Work You will own audit-readiness across RDI's diagnostic studies and help lead a team of junior CRAs and data-entry team members.
- Can you build a world-class team of IVD CRAs?
- You will own monitoring quality and audit-readiness across RDI's diagnostic studies.
- You will develop the systems that demonstrate study quality and status to leadership and, where appropriate, to clients.
Requirements
- You need real knowledge of the regulations and monitoring standards.
- The ideal candidate already knows what that means and has likely built or operated a system that keeps multiple studies inspection-ready at once.
Benefits
- Remote candidates will be considered only if they have a proven method for learning our business, applying our standards, and managing quality across a remote team.
Company info
- RDI is a small, merit-based company, and no leader here gets to stay above the work.
This listing is sourced directly from RDI's careers page and normalized into a canonical job model.