Research Coordinator – Data, IRB & Study Ops
ultiproBaton Rouge (LA)
Research Coordinator – Data, IRB & Study Ops
Posted today
ultiproBaton Rouge (LA)
Clinical Research CoordinatorsResearch and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)
SENIORITY
Mid
About the role
Woman’s Hospital in Baton Rouge, LA is seeking a Research Coordinator to oversee and execute study protocols, manage data, obtain informed consent, and communicate study status across teams including nurses and principal investigators.
You will coordinate visits, assist with regulatory submissions, and support data quality through REDCap projects, case report forms, and data auditing, contributing to high-quality clinical research in a large women's hospital setting.
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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