Job Description
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.
All Job Postings will close at 12:01a.m. CST (1:01a.m. EST) on the specified Closing Date (if designated). If you close the browser or exit your application prior to submitting, the application progress will be saved as a draft. You will be able to access and complete the application through "My Draft Applications" located on your Candidate Home page. Job Posting Title: Research Nurse
Position Type: Professional / Unclassified
Department: LSUPBRC Cores - CTU - Clinical Trials Operations (Melissa Lingle (00002335))
Work Location: LSU - Pennington Biomedical
Pay Grade: Professional Hourly
: Pennington Biomedical Research Center, a world-renowned academic research institute of Louisiana State University, is seeking a Research Nurse in the Clinical Trials Unit.
Make an impact in advancing medical research while delivering exceptional patient care. Join our dynamic team in the Clinical Trials Unit as a Research Nurse and play a pivotal role in groundbreaking studies that shape the future of healthcare.
Job Responsibilities - Collect, document, and analyze participant adherence to study drug protocols.
- Monitor ongoing compliance through direct observation, participant interviews, and data review, and implement interventions as needed to support adherence.
- Administer injectable investigational products in accordance with study protocols and institutional guidelines.
- Monitor participants for immediate adverse reactions and document all administration activities accurately.
- Provide individualized education and counseling to participants regarding study drug use, potential side effects, and the importance of compliance.
- Deliver personalized education sessions to participants, explaining study drug usage, potential side effects, and compliance expectations.
- Serve as a trusted resource for participants, addressing questions and concerns to promote understanding and engagement throughout the trial.
- Oversee regulatory aspects of clinical trial operations, including IRB submissions, protocol amendments, and compliance with Good Clinical Practice (GCP) standards.
- Coordinate the implementation of study protocols in collaboration with investigators and institutional departments to ensure regulatory and operational readiness.
- Manage all regulatory submissions, including IRB applications, continuing reviews, and protocol amendments, ensuring accuracy and timeliness.
Required Qualifications - BSN required or ADN with equivalent clinical experience in research or specialty care.
- Current Registered Nurse (RN) license in the state of Louisiana.
- Minimum 1 year of clinical nursing experience, preferably in research or specialty care.
- Strong skills in participant education, counseling, and adherence monitoring.
- Proficiency in electronic data capture systems and clinical documentation.
- Excellent organizational, communication, and interpersonal skills.
- Ability to work independently and collaboratively in a multidisciplinary team environment.
Preferred Qualifications
- Experience in clinical research nursing or working in clinical trials.
- Familiarity with IRB submissions, regulatory documentation, and protocol development.
- Prior experience in participant recruitment and retention strategies.
- Knowledge of clinical trial management systems (CTMS) and regulatory platforms (e.g., REDCap).
- CCRP (Certified Clinical Research Professional) or CCRC (Certified Clinical Research Coordinator).
Pennington Biomedical Research Center (PBRC) is an equal employment opportunity employer and serves as a model employer for individuals with disabilities.
Additional : Why You'll Love This Role
- Be part of innovative research that directly impacts patient outcomes and advances medical knowledge.
- Work in a collaborative environment with leading investigators and multidisciplinary teams.
- Enjoy professional growth opportunities through exposure to cutting-edge clinical trials and regulatory processes.
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: January 9, 2026
Closing Date (Open Until Filled if No Date Specified): January 26, 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 [click to reveal email address] 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 [click to reveal phone number]225-763-2776 or [click to reveal email address] hrm@pbrc.edu .
Job Tags
Hourly pay, Full time, Immediate start, Flexible hours,