Clinical Research Coordinator 1 - Brain and Metabolism Imaging
Louisiana State UniversityAbout the role
About Us:
At the forefront of medical discovery as it relates to understanding the causes of obesity, diabetes, cardiovascular disease, cancer and dementia, Pennington Biomedical Research Center is a campus of Louisiana State University and conducts basic, clinical and population research. The Center includes Basic Science, Clinical Research, and Population and Public Health, enabling both focused research and translational science. Research at Pennington Biomedical is supported broadly by multiple NIH Research Centers, and includes approximately 65 faculty and 20 postdoctoral fellows who comprise a network of 44 laboratories and 13 highly specialized core service facilities. Pennington Biomedical is located within state-of-the-art research facilities on a 222-acre campus in Baton Rouge, Louisiana.
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Job Posting Title:
Clinical Research Coordinator 1 - Brain and Metabolism Imaging
Position Type:
Professional / Unclassified
Department:
LSUPBRC Clinic - Brain and Metabolism Imaging in Chronic Disease (Owen T Carmichael (00007151))
Work Location:
LSU - Pennington Biomedical
Pay Grade:
Professional
Job Description:
Pennington Biomedical Research Center, a world-renowned academic research institute of Louisiana State University, is seeking a Clinical Research Coordinator 1 in the Brain and Metabolism Imaging in Chronic Disease Laboratory.
The Clinical Research Coordinator will oversee and participate in medical, clinical and interventional research studies as per established protocols and institutional policies and procedures. They will organize and coordinate the screening, consenting, and scheduling aspects of research studies; ensure effective participant interactions and communication, especially via telephone calls. This position offers a unique opportunity to coordinate participant-centered research while contributing to scientific research.
Major Responsibilities
Coordinate and execute study activities in collaboration with the project manager, data manager, investigators, and research team to ensure study milestones, recruitment targets, and project deliverables are achieved according to established timelines.
Coordinate and conduct participant screening, eligibility determination, informed consent discussions and documentation, enrollment, and study visit coordination in accordance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
Maintain accurate, complete, and timely study records within electronic data capture systems; perform data quality reviews, query resolution, and source document verification to ensure data integrity and protocol compliance.
Assist with the preparation, maintenance, and organization of regulatory and study-related documents, including study protocols, manuals of procedures, training materials, recruitment materials, and Institutional Review Board (IRB) submissions.
Generate and maintain study reports, recruitment metrics, safety reports, progress updates, and other project documentation for investiga
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