Clinical Research Study Coordinator

Louisiana State University

20h•Onsite

About The Position

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. Pennington Biomedical Research Center, a world-renowned academic research institute of Louisiana State University, is seeking a Clinical Research Study Coordinator in the Clinical Trials Unit. The Clinical Research Study Coordinator supports the execution of clinical trials within the Clinical Trials Unit by assisting with day-to-day study activities. This entry-level role provides essential coordination of research operations, including participant engagement, data collection, and regulatory support. The position is ideal for individuals with a strong interest in clinical research, healthcare, or scientific advancement, and offers foundational experience in the conduct of clinical trials under established protocols and regulatory guidelines.

Requirements

Bachelor’s degree (or in progress) in a health, science, or related field
Strong interest in clinical research or healthcare
High attention to detail and organizational skills
Ability to follow protocols and work in a regulated environment
Strong communication and interpersonal skills
Proficiency with basic computer applications and data entry
Current CPR certification or willingness to complete course after hiring

Responsibilities

Assist with the coordination and implementation of clinical research studies in accordance with study protocols, institutional policies, and regulatory requirements.
Collect, enter, and maintain accurate clinical and research data in study databases.
Ensure proper documentation and maintenance of study records, including regulatory binders and participant files.
Monitor study activities to ensure compliance with protocols, informed consent processes, and participant safety standards.
Coordinate study-related procedures, including laboratory tests, specimen handling, and data collection activities.
Communicate with study participants, investigators, and clinical staff to facilitate smooth study operations.
Assist with preparation for monitoring visits, audits, and inspections.
Perform other administrative and research support duties as assigned.