LSU

Clinical Research Study Coordinator

LSU - Pennington Biomedical Full time

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 Study Coordinator

Position Type:

Professional / Unclassified

Department:

LSUPBRC Cores - CTU - Clinical Trials Operations (Melissa Lingle (00002335))

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 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.

Job 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.

Required Qualifications

  • 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

Pennington Biomedical Research Center seeks to recruit a highly productive workforce with a broad range of backgrounds and perspectives and will provide equal employment opportunities to all employees and prospective employees. Employment decisions shall be based strictly on merit and without regard to religious or political beliefs, sex, race, or any other non-merit factor.

Additional Job Description:

Competencies:

None

Special Instructions:

Interested candidates should include a resume and a list of three (3) professional references to the online application. Professional references should be the name, title, company, and contact information from past employers. Professional references should include current or previous supervisors and/or coworkers. Personal references should not be considered for the reference check process. We will respect the request that we not contact a current employer. However, we will need to contact a prior supervisor if such a request is made.

A letter of application/cover letter is recommended but not required. Official transcripts are required prior to hire and are not required at the time of application.

Posting Date:

April 20, 2026

Closing Date (Open Until Filled if No Date Specified):

May 4, 2026

Additional Position Information:

Pennington Biomedical is located within state-of-the-art research facilities on a 222-acre campus in Baton Rouge, Louisiana. For more information, visit PBRC.

Questions regarding career opportunities at Pennington Biomedical should be sent to hrm@pbrc.edu.

Background Check - An offer of employment is contingent on a satisfactory pre-employment background check.

Benefits - Pennington Biomedical Research Center offers outstanding benefits to eligible employees and their dependents including health, life, dental, and vision insurance; flexible spending accounts; retirement options; various leave options; paid holidays; wellness benefits; tuition exemption for qualified positions; training and development opportunities; employee discounts; and more!

   

Positions approved to work outside the State of Louisiana shall be employed through Louisiana State University’s partner, nextSource Workforce Solutions, for Employer of Record Services including but not limited to employment, benefits, payroll, and tax compliance. Positions employed through Employer of Record Services will be offered benefits and retirement as applicable through their provider and will not be eligible for State of Louisiana benefits and retirement.

   

Essential Position (Y/N):

   

Pennington Biomedical Research Center/LSU is an Equal Opportunity Employer.

   

Contact Information:

Questions or concerns can be directed to PBRC Human Resources at 225-763-2776 or hrm@pbrc.edu.