What are the responsibilities and job description for the Clinical Monitoring Standards Lead position at RDI - Your IVD CRO?
The Role
Can you build a world-class team of IVD CRAs?
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 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.
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.
You need real knowledge of the regulations and monitoring standards. If your understanding comes mainly from checklists, templates, or PowerPoints someone else made for you, this is not the right role.
This role is for a master of the craft: someone who can do the work, teach the work, inspect the work, and hold a team to the standard.
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.
The ideal candidate already knows what that means and has likely built or operated a system that keeps multiple studies inspection-ready at once.
This is not traditional management. RDI is a small, merit-based company, and no leader here gets to stay above the work.
You will dig into the details: reviewing an individual informed consent, checking source against CRF data, walking through query status, reviewing a binder, or finalizing a monitoring report alongside the team.
You are accountable for the standard holding in real work, not just existing in a document.
Location and Schedule
This role is strongest if based near our Los Angeles / Van Nuys office.
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.
About RDI
RDI is one of the fastest-growing IVD-focused CROs in the industry. We work on difficult diagnostic studies for some of the largest IVD manufacturers in the world.
We have built a small team intentionally and seek people with true ownership, high standards, and a dedication to excellence.
About Our Process
Our recruiting process is management-led. If your application and background fit, either the CEO or COO will reach out directly for a phone screen.
Given the volume of applicants, we cannot reply to everyone, but we reply to every strong application.
Can you build a world-class team of IVD CRAs?
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 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.
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.
You need real knowledge of the regulations and monitoring standards. If your understanding comes mainly from checklists, templates, or PowerPoints someone else made for you, this is not the right role.
This role is for a master of the craft: someone who can do the work, teach the work, inspect the work, and hold a team to the standard.
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.
The ideal candidate already knows what that means and has likely built or operated a system that keeps multiple studies inspection-ready at once.
This is not traditional management. RDI is a small, merit-based company, and no leader here gets to stay above the work.
You will dig into the details: reviewing an individual informed consent, checking source against CRF data, walking through query status, reviewing a binder, or finalizing a monitoring report alongside the team.
You are accountable for the standard holding in real work, not just existing in a document.
Location and Schedule
This role is strongest if based near our Los Angeles / Van Nuys office.
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.
About RDI
RDI is one of the fastest-growing IVD-focused CROs in the industry. We work on difficult diagnostic studies for some of the largest IVD manufacturers in the world.
We have built a small team intentionally and seek people with true ownership, high standards, and a dedication to excellence.
About Our Process
Our recruiting process is management-led. If your application and background fit, either the CEO or COO will reach out directly for a phone screen.
Given the volume of applicants, we cannot reply to everyone, but we reply to every strong application.
Salary : $115,000 - $135,000