LCMC Health
Location
New Orleans, Louisiana
The role manages regulatory documents and submissions to pharmaceutical sponsors, IRBs, and CROs to implement clinical trials. It also involves coordinating audits, performing quality assurance, and mentoring junior staff members.
Requires 5 years of experience in clinical research and an Associate's degree, though 7 years of experience can substitute for education. A Bachelor's degree and previous experience as a regulatory coordinator are preferred.
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