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Clinical Research Rn Jobs in Baton Rouge, LA (NOW HIRING)

TNAA TotalMed RN is seeking a travel nurse RN Electrophysiology Lab for a travel nursing job in ... clinicians of all specialties in all 50 states. They offer local and travel jobs and match ...

Here is your chance to join our dynamic healthcare team as a Clinical Supervisor RN in Baton Rouge, LA . Why Join Us? At STAT Home Health , we invest in our people through an Employee Stock Ownership ...

Here is your chance to join our dynamic healthcare team as a Clinical Supervisor RN in Baton Rouge, LA . Why Join Us? At STAT Home Health , we invest in our people through an Employee Stock Ownership ...

Pathways, Training & Advancement Officer Development School followed by orientation and clinical ... research, and staff positions; access to leadership courses and Navy funded graduate education for ...

Pathways, Training & Advancement Officer Development School followed by orientation and clinical ... research, and staff positions; access to leadership courses and Navy funded graduate education for ...

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Clinical Research Rn information

See Baton Rouge, LA salary details

$17

$42

$60

How much do clinical research rn jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for clinical research rn in Baton Rouge, LA is $42.38, according to ZipRecruiter salary data. Most workers in this role earn between $34.86 and $50.34 per hour, depending on experience, location, and employer.

What is a clinical research RN?

Clinical Research Registered Nurses (Clinical Research RNs) are licensed nurses who specialize in conducting and coordinating clinical trials and research studies involving human participants. They collaborate with physicians, researchers, and study coordinators to ensure that research protocols are followed, participants are cared for safely, and all regulatory and ethical guidelines are met. Their duties include administering study medications, collecting data, monitoring patient responses, and educating participants about the study. Clinical Research RNs play a vital role in advancing medical knowledge and improving patient care through research.

How does a clinical research RN typically collaborate with other members of the research team?

A Clinical Research RN works closely with principal investigators, study coordinators, physicians, and data managers to ensure research protocols are followed accurately and patient safety is maintained. They are responsible for communicating patient progress, reporting adverse events, and coordinating care between departments. Regular team meetings and detailed documentation are essential to keep everyone informed and maintain compliance with regulatory standards. This collaborative environment helps ensure research studies run smoothly and efficiently.

What are the key skills and qualifications needed to thrive as a clinical research RN, and why are they important?

To thrive as a Clinical Research RN, you need a solid background in nursing, clinical trial protocols, and regulatory compliance, typically requiring an RN license and experience in research settings. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often expected. Excellent organizational, communication, and critical thinking skills help you coordinate studies, interact with participants, and collaborate with multidisciplinary teams. These competencies ensure the integrity of research data, patient safety, and successful execution of clinical trials.

What is the difference between Clinical Research Rn vs Clinical Research Coordinator?

AspectClinical Research RnClinical Research Coordinator
CredentialsRN license, possibly specialized certificationsTypically bachelor's degree, certifications like CCRP beneficial
Work EnvironmentHospitals, clinics, research institutionsResearch sites, hospitals, clinics
Job FocusPatient care, protocol adherence, data collectionStudy coordination, participant recruitment, data management

While both roles are involved in clinical research, the Clinical Research Rn primarily provides patient care and ensures protocol compliance from a nursing perspective. The Clinical Research Coordinator manages study logistics, participant recruitment, and data collection. Both roles require strong organizational skills, but the RN's focus is more on patient interaction, whereas the Coordinator handles study operations.

How to get into clinical research as a registered nurse?

To become a clinical research RN, obtain a valid nursing license and gain experience in patient care. Additional certifications such as Certified Clinical Research Professional (CCRP) or Good Clinical Practice (GCP) training can improve job prospects, and familiarity with research protocols and data management is beneficial.

What do clinical research RNs do in clinical research?

Clinical research RNs coordinate and monitor clinical trials by recruiting participants, collecting data, administering treatments, and ensuring compliance with study protocols and regulations. They often work closely with investigators, maintain accurate documentation, and may require certification such as CCRP. Their role is essential for the safe and effective conduct of research studies.

What are popular job titles related to Clinical Research Rn jobs in Baton Rouge, LA?

For Clinical Research Rn jobs in Baton Rouge, LA, the most frequently searched job titles are:

What cities near Baton Rouge, LA are hiring for Clinical Research Rn jobs?

Cities near Baton Rouge, LA with the most Clinical Research Rn job openings:

Infographic showing various Clinical Research Rn job openings in Baton Rouge, LA as of August 2026, with employment types broken down into 3% As Needed, 75% Full Time, 15% Part Time, and 7% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $88,147 per year, or $42.4 per hour.

Clinical Research Coordinator 1

Louisiana State University

Baton Rouge, LA โ€ข On-site

$21 - $27.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement

This job post hasย expired today.ย Applications are no longer accepted.


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:
Clinical Research Coordinator 1
Position Type:
Professional / Unclassified
Department:
LSUPBRC PopSci - Physical Activity Epidemiology - Clinical Studies (Kara D Denstel (00000631))
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 Population and Public Health Sciences.
Pennington Generation is a longitudinal cohort study enrolling children and adolescents and their families from throughout Louisiana and following them over time to better understand the causes and consequences of the development of obesity and other chronic conditions. The Clinical Research Coordinator will be responsible for the implementation of this statewide cohort study. The Clinical Research Coordinator will work with a team who are responsible for the maintenance and implementation of study documents (protocols, manuals of procedure, Institutional Review Board materials, etc.), participant informed consent and screening, recruitment, assessment, and retention of participants in studies, safety monitoring, data monitoring, and overall study conduct. The position will require frequent statewide travel on a mobile health unit on
which the study visits and other study procedures will take place.
Major Responsibilities
  • Coordinate and conduct study recruitment, participant screening, informed consent, enrollment, and follow-up activities in accordance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
  • Travel throughout Louisiana to implement study visits and collect high-quality research data in community settings and aboard a mobile health unit, including both single-day and multi-day trips.
  • Build and maintain relationships with participants, community partners, and stakeholders to support recruitment, engagement, and long-term participant retention.
  • Manage study documentation, regulatory records, electronic data capture systems, and data quality activities to ensure accurate, complete, and compliant study conduct.
  • Collaborate with investigators and research team members to achieve study milestones, prepare study reports and materials, support monitoring and audit activities, and contribute to the successful execution of a large-scale longitudinal research study.

Required Qualifications
  • Bachelor's degree in Public Health, Health Sciences, Biological Sciences, Psychology, Kinesiology, Nursing, Nutrition, Social Sciences, or a related field.
  • One (1) year of experience in clinical research, healthcare, public health, community-based research, participant recruitment, or a related field which can include internships, academic research, or work in a clinical or research lab setting.
  • Experience interacting with research participants, patients, clients, or community members in a professional setting.
  • Strong organizational, time management, and project coordination skills with the ability to manage multiple priorities and meet deadlines.
  • Excellent written and verbal communication skills and the ability to work effectively with diverse populations, community partners, investigators, and research staff.
  • Proficiency with Microsoft Office applications and the ability to learn electronic data capture and research management systems.
  • Ability and willingness to travel extensively throughout Louisiana, including occasional overnight travel, and prossess a valid driver's license with an acceptable driving record.

Preferred Qualifications
  • Demonstrated ability to collect, document, and maintain accurate records and data with strong attention to detail.
  • Knowledge of Good Clinical Practice (GCP), human subjects protections, informed consent procedures, and Institutional Review Board (IRB) requirements.
  • Experience using electronic data capture systems (e.g., REDCap), clinical trial management systems, or other research databases.

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:
August 14, 2026
Closing Date (Open Until Filled if No Date Specified):
August 28, 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.