Impactful Research Regulatory Specialist; Clinical Trials
Listed on 2026-09-30
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Research/Development
Clinical Research, Regulatory Compliance Specialist
LCMC Health in New Orleans seeks a Regulatory Coordinator to manage regulatory documents for clinical studies, prepare sponsor/CRO submissions, and maintain IRB materials. The role supports audits and ensures compliance across trials.
The candidate should have 2 years of clinical research experience and an Associate’s degree;
SoCRA/ACRP certification is preferred. This on-site position collaborates with investigators and staff across departments.
We invite applications for the Impactful Research Regulatory Specialist (Clinical Trials) position located in KY, United States.
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This posting is for the Impactful Research Regulatory Specialist (Clinical Trials) role at LCMC Health, based in KY, United States.
We are looking to fill the Impactful Research Regulatory Specialist (Clinical Trials) position at LCMC Health in KY, United States.
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