Research Nurse - Clinical Trials Outpatient Unit

## Research Nurse - Clinical Trials Outpatient UnitApplylocations: LSU - Pennington Biomedicaltime type: Full timeposted on: Posted Todaytime left to apply: End Date: June 9, 2026 (13 days left to apply)job requisition id: R00115886## 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 - Clinical Trials Outpatient Unit## 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 Research Nurse in the Clinical Trials Outpatient Unit.Join a collaborative outpatient clinical research team dedicated to advancing innovative treatments and improving patient outcomes. The Research Nurse supports clinical trial activities, including participant care, investigational product administration, protocol compliance, patient education, and regulatory documentation. This role offers the opportunity to combine direct patient care with cutting-edge research in a fast-paced and mission-driven environment focused on excellence, compassion, and scientific discovery. ***Major Responsibilities**** Coordinate and deliver outpatient clinical trial activities in collaboration with investigators, sponsors, and interdisciplinary teams to ensure protocol compliance, participant safety, and high-quality research outcomes.* Administer investigational medications and injectable study products in accordance with study protocols, institutional policies, and regulatory requirements while closely monitoring participants for adverse reactions and documenting all activities accurately and thoroughly.* Monitor participant adherence to study drug protocols through direct observation, participant interviews, data review, and ongoing follow-up, implementing supportive interventions and education strategies to optimize compliance and study retention.* Provide individualized education and counseling to research participants regarding study procedures, investigational treatments, medication administration, potential side effects, and the importance of protocol adherence, fostering participant engagement and trust throughout the clinical trial experience.* Serve as a primary clinical resource for participants by addressing questions, assessing concerns, coordinating care needs, and promoting a positive and supportive research experience from enrollment through study completion.* Oversee regulatory and compliance activities for assigned clinical trials, including preparation and submission of IRB applications, continuing reviews, protocol amendments, and essential regulatory documents in accordance with Good Clinical Practice (GCP), sponsor requirements, and institutional standards.* Collaborate with investigators, research staff, pharmacy, laboratory, and institutional departments to facilitate successful study activation, protocol implementation, and ongoing operational readiness for outpatient clinical research studies.* Maintain accurate, timely, and complete clinical research documentation, ensuring data integrity, participant confidentiality, and readiness for sponsor audits, monitoring visits, and regulatory inspections.***Required Qualifications**** Bachelor’s degree in Nursing (BSN) *or* Associate’s degree in Nursing (ASN) with equivalent clinical experience in research or specialty care.* Current, unrestricted Registered Nurse (RN) licensure in Louisiana.* Minimum of one (1) year of nursing experience in a clinical setting.* Strong clinical assessment skills with the ability to recognize, evaluate, and respond to adverse events and participant safety concerns.* Demonstrated ability to educate and counsel participants regarding study procedures, medications, side effects, and protocol compliance using clear and compassionate communication.* Excellent organizational, time management, and multitasking skills with the ability to manage multiple studies and priorities in a fast-paced outpatient research environment.* Strong interpersonal and collaboration skills with the ability to work effectively with investigators, sponsors, research staff, and interdisciplinary healthcare teams.* Proficiency in electronic medical records (EMR), clinical documentation systems, and Microsoft Office applications.* Ability to maintain strict confidentiality, data integrity, and compliance with institutional, sponsor, and regulatory requirements.***Preferred Qualifications**** Three (3) years of nursing experience in clinical research, outpatient care, oncology, infusion services, ambulatory care, or other related clinical specialty.* Experience coordinating or supporting clinical trials, research protocols, or investigational drug studies.* Knowledge of Good Clinical Practice (GCP), Institutional Review Board (IRB) processes, FDA regulations, and human subject protection standards.*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:May 26, 2026## Closing Date (Open Until Filled if No Date Specified):June 9, 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 View email address on click.appcast.io.**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. #J-18808-Ljbffr