About the role

Sarah Cannon Research Institute (SCRI) seeks a Manager of Research Regulatory Affairs to oversee regulatory operations for SCRI and manage the Regulatory Department. You will develop and implement strategies to ensure FDA and GCP compliance across multiple clinical trials, coordinating audits with sponsors and government agencies. You will lead a team, establish procedures, and partner with investigators and industry sponsors to maintain regulatory excellence in clinical operations.

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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