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Clinical Research Assistant Jobs in Baton Rouge, LA

The Center includes Basic Science, Clinical Research, and Population and Public Health, enabling both focused research and translational science. Research at Pennington is supported broadly by ...

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Clinical Research Assistant information

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$7

$19

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How much do clinical research assistant jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for clinical research assistant in Baton Rouge, LA is $19.87, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $22.69 per hour, depending on experience, location, and employer.

What is a clinical research assistant?

Clinical Research Assistants are professionals who support clinical research studies by performing a range of administrative and research-related tasks. They help collect and manage data, assist with patient recruitment, prepare study materials, and ensure compliance with research protocols and regulations. Their work is crucial in advancing medical knowledge and ensuring that clinical trials run smoothly and ethically. Clinical Research Assistants often work under the supervision of principal investigators or clinical research coordinators in hospitals, universities, or pharmaceutical companies.

What does a clinical research assistant do?

A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.

What are the key skills and qualifications needed to thrive as a clinical research assistant?

To thrive as a Clinical Research Assistant, you need a bachelor’s degree in a life science or health-related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) certification are typically required. Excellent communication, teamwork, and problem-solving abilities help you excel in coordinating with research teams and participants. These skills ensure accurate data collection, regulatory compliance, and the smooth execution of clinical studies.

What are some common challenges clinical research assistants face when coordinating multiple studies simultaneously?

Clinical Research Assistants often manage several studies at once, which can lead to challenges in balancing competing deadlines, maintaining accurate documentation, and ensuring compliance with complex protocols. Effective time management and organizational skills are crucial to handle overlapping tasks such as scheduling patient visits, collecting data, and preparing regulatory submissions. Collaborating closely with principal investigators, coordinators, and other team members helps distribute the workload and maintain research quality. Developing strong communication habits and utilizing digital tracking tools can further streamline workflow and reduce errors.

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

AspectClinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentAssists in data collection, patient scheduling, and administrative tasks in clinical trial settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trial sites
Employer & IndustryHospitals, research institutions, pharmaceutical companiesHospitals, research centers, pharmaceutical companies

Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

Can you be a clinical research assistant with no experience?

Clinical research assistant positions often require some knowledge of medical terminology and data management, but many entry-level roles are available for candidates without prior experience. Employers may provide on-the-job training and look for strong organizational skills, attention to detail, and the ability to follow protocols. Certifications such as Good Clinical Practice (GCP) can enhance prospects for those new to the field.

What are the most commonly searched types of Clinical Research jobs in Baton Rouge, LA?

The most popular types of Clinical Research jobs in Baton Rouge, LA are:

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

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

Infographic showing various Clinical Research Assistant 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 $41,334 per year, or $19.9 per hour.

Clinical Research Coordinator 1

Louisiana State University

Baton Rouge, LA • On-site

$21 - $27.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 13 days ago


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.