Senior Clinical Research Associate

RDI

Job Overview

Location

Van Nuys, California, United States

Salary

USD 80,000 - 130,000 annual

Employment Type

Full-time

Work Arrangement

On-site

Sector

Healthcare & Medical

Experience Level

Senior (5-8 years)

Application Deadline

April 20, 2026

About the Company

RDI is at the forefront of IVD (In Vitro Diagnostics) product validation, offering comprehensive support throughout the development pathway. Leveraging a diverse physician network and a high-complexity CLIA lab, RDI delivers reliable and accelerated solutions for IVD development.

With a proven track record of completing nearly 200 trials and over 15 years of experience, RDI combines a technologically forward approach with deep industry expertise. The company is dedicated to guiding clients through their IVD development process, accelerating research, and delivering quality outcomes.

Job Description

RDI is seeking a dedicated Senior Clinical Research Associate to spearhead IVD diagnostic clinical studies from initiation to completion. In this pivotal role, you will be instrumental in driving studies forward, taking full ownership of the process rather than merely reporting on it.

At RDI, we foster a culture of direct impact and problem-solving. We are a team that thrives in dynamic, high-stakes environments where initiative and grit are paramount. We value individuals who are driven to figure things out and who possess an unwavering commitment to doing work that truly matters.

We are looking for individuals who are not just seeking a career, but a place to make a tangible difference. If you are ready to take on significant responsibility and contribute to groundbreaking diagnostic advancements, RDI offers a unique opportunity for growth and impact.

To apply for this role, click the Apply button on this page and follow the instructions.

Required Skills

Clinical Trial ManagementSite ActivationData LockIVD StudiesRegulatory ComplianceData Integrity

Key Responsibilities

Own IVD diagnostic clinical studies end-to-end, from site activation through data lock.
Manage multiple active trials concurrently.
Drive study progress and ensure successful execution.
Collaborate with sites and internal teams to overcome challenges.
Maintain high standards of data integrity and regulatory compliance.

Qualifications

Three or more years of hands-on CRA or CRC experience where you owned studies, not supported them.
IVD, device, or diagnostics background strongly preferred.
Experience in environments requiring independent problem-solving.
Grit and a strong sense of personal accountability.

Benefits & Perks

Opportunity to own critical clinical studies.
Work in a fast-paced, high-impact environment.
Clear path to project management through performance.
Competitive salary based on experience and contribution.

How to Apply

Answer three questions that describe real situations in this role.

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The IVD diagnostics sector is experiencing rapid expansion, driven by advancements in early disease detection. This role demands end-to-end ownership of clinical studies, from site activation to data lock, managing multiple trials concurrently. Key technical skills include clinical trial management, regulatory compliance, data integrity, and site monitoring. The impact of this position is significant, directly influencing RDI's ability to bring life-saving diagnostic tests to market and contributing to the company's growth and leadership in a high-stakes, fast-paced industry.