Clinical Trial Manager or Senior CRA - Diagnostics CRO (On-site)

About This Role

You should already know what this job entails — startup, monitoring, data, sites, timelines, and clients. Here at RDI, you own all of it.

You’ll manage diagnostic clinical studies end to end — qualifying sites, designing and distributing kits, monitoring data integrity, managing site communications, and ensuring delivery to the client and lab. You’ll operate across lab, clinical, regulatory, and sponsor functions as one integrated system.

No layers. No committees. No one to hide behind.

About RDI

RDI is the CRO for the most powerful and innovative diagnostic companies in the world.

They come to us to accelerate or save their study timelines. Founded in 2008, have run 300+ trials and counting, and are growing at an unprecedented rate.

For the right person, there has never been a better time to join.

Our Culture

We are not a family — much closer to a tight knit sports team trying to make the Olympics or playoffs. The odds have been against us, but we have won through grit, preparation, and trust in each other’s excellence.

Everyone pulls their weight. Everyone practices. Everyone wants the ball.

You’ll work hard here — the timelines are tight, the expectations are high — and you’ll still show up for clients with professionalism and energy. We want happy warriors , not bitter ones.

We won’t be offended if you prefer comfort, predictability, and the trappings of a large company — those places have their merits. But if you’d rather build, compete, and win  alongside people who hold themselves to a higher standard, come on in.

Our team culture is precious and we screen new candidates rigorously. Hundreds of applicants apply and we will wait months for the right one. Excellence is worth waiting for.

Requirements

• Bachelor's degree in life sciences, nursing, or a related field; advanced degree preferred.
• At least 2 years of experience as a Clinical Research Associate or similar role in the clinical research industry.
• The ability to travel up to 30%.
• Strong knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
• Excellent communication, interpersonal, and presentation skills.
• Ability to travel to various clinical sites as required by the study protocol.
• Strong organizational skills and attention to detail in managing multiple priorities.
• Proficient in using clinical trial management systems (CTMS) and other relevant technologies.

Benefits