About the role

Celerion is seeking a qualified Principal Investigator to oversee safety and conduct of clinical trials in line with FDA, GCP, and IRB requirements. The PI ensures subject safety, protocol adherence, and accurate data collection during all study phases. Responsibilities include protocol review, subject screening, SAE assessment, case report forms, safety reporting, and collaboration with sponsors and IRB. Candidates should have MD/DO, active license, and relevant clinical research experience,

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.

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