Clinical Research Compliance Specialist (Hybrid)

Posted 2 days ago

university of southern californiaLos Angeles (CA)

SENIORITY

Lead

Apply

About the role

University of Southern California is seeking a Regulatory Compliance professional to support the Clinical Investigations Support Office. You will manage protocols, informed consent documents and regulatory filings while ensuring adherence to IRB and FDA requirements. You will coordinate with investigators, sponsors, and staff, preparing reviews, training materials, and audits to promote high-quality research and subject protection. This is a hybrid position based in Los Angeles.

Before you apply

Applying takes about a minute. These four things decide how fast it moves after that.

Your profile is current

It's what we read first. Occupations, seniority and locations matter more than a long history.

Two examples you can talk through

Not a portfolio — just two pieces of work where you can explain the decisions and what you'd change.

A number in mind

What you're on now and what would make you move. We negotiate better when we know both.

Your notice period

Employers plan around it, and it's the question that stalls offers most often.

Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.

More like this