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Clinical Trials Assistant Jobs in Baton Rouge, LA

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Clinical Trials Assistant information

See Baton Rouge, LA salary details

$11

$19

$27

How much do clinical trials assistant jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for clinical trials assistant in Baton Rouge, LA is $19.43, according to ZipRecruiter salary data. Most workers in this role earn between $15.91 and $22.40 per hour, depending on experience, location, and employer.

What is a clinical trials assistant?

Clinical Trials Assistants (CTAs) are professionals who support the planning, coordination, and administration of clinical trials, which are research studies that evaluate the safety and effectiveness of medical treatments or interventions. They handle tasks such as maintaining trial documentation, assisting with regulatory submissions, scheduling meetings, and ensuring data accuracy. CTAs play a crucial role in helping clinical research teams comply with protocols and regulatory requirements, making the clinical trial process run smoothly and efficiently.

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

To thrive as a Clinical Trials Assistant, you need a solid understanding of clinical research processes, regulatory guidelines, and attention to detail, often supported by a degree in life sciences. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, effective communication, and the ability to multitask make candidates stand out in this role. These skills are essential for ensuring compliance, accurate documentation, and the smooth execution of clinical studies.

What are some typical challenges a clinical trials assistant faces during a study, and how can they be managed?

Clinical Trials Assistants often encounter challenges such as managing large volumes of documentation, ensuring timely data entry, and coordinating communication among multiple stakeholders. Staying organized and using established tracking systems can help manage documents efficiently. Proactive communication and regular check-ins with team members—such as study coordinators and data managers—are key to resolving issues quickly and maintaining study timelines. Embracing good time management practices and seeking mentorship from senior staff can further ease these common challenges.

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

AspectClinical Trials AssistantClinical Research Coordinator
CredentialsHigh school diploma or equivalent; some roles may require certificationBachelor’s degree in health sciences or related field; often requires certification
Work EnvironmentResearch sites, hospitals, clinics, pharmaceutical companiesResearch sites, hospitals, clinics, pharmaceutical companies
ResponsibilitiesAssist with data entry, document management, and trial logisticsOversee trial processes, patient recruitment, data collection, and compliance
Industry UsageCommonly used in clinical trial support rolesMore involved in trial management and coordination

While both roles support clinical trials, Clinical Trials Assistants focus on administrative and logistical tasks, whereas Clinical Research Coordinators handle more comprehensive trial management, patient interactions, and compliance activities.

How to become a clinical trials assistant?

To become a clinical trials assistant, candidates typically need a high school diploma or equivalent, with some roles preferring post-secondary education in health or science fields. Relevant skills include attention to detail, organization, and familiarity with clinical trial protocols and documentation. Gaining experience through internships or entry-level positions in healthcare or research settings can also improve job prospects.

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

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

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

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

Infographic showing various Clinical Trials Assistant job openings in Baton Rouge, LA as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 14% Part Time, 2% Temporary, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $40,406 per year, or $19.4 per hour.

Director of Clinical Operations

Pennington Biomedical Research Center

Baton Rouge, LA • On-site

$120 - $160/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 3 days ago

New


Job description

Director of Clinical Operations

Apply Full time 5 days ago R00119284

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.

Job Posting Title:

Director of Clinical Operations

Position Type:

Professional / Unclassified

Department:

LSUPBRC ExD - Core Resources Services (Jennifer Rood (00000102) (Inherited))

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 Director of Clinical Operations in the Clinical Trials Unit.

The Director of Clinical Operations coordinates all operational and logistical processes associated with the inpatient and outpatient clinic. This includes coordination of research programs, implementing and initiating proposed clinical programs, and serving as primary contact for community-based research initiatives and networking projects.

Major Responsibilities
  • Coordinate and oversee the overall operation of the clinic.
  • Work collaboratively with members of the team (consisting of the principal investigators, research study assistants, data managers, nursing and administrative staff) in theclinic.
  • Works on the development and implementation of new employee training and orientation programs.
  • Provides status reports on the operation of the Clinical Trials Unit; ensures effective communication regarding study completion, resource utilization, study status, and quality improvement results.
  • Communicates with other members of the Clinical Trials Unit management team to ensure effective and efficient operation and continuity of research services.
  • Attends individual study meetings as requested/required.
  • Represents the Clinical Trials Unit on all committees and institutional meetings as requested.
Required Qualifications
  • Master's degree in business administration or health related field.
  • 10 or more years of experience in medical management/administration.

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.

Posting Date:

August 20, 2026

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

September 21, 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.

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 .

Centers & Institutes

Metabolic Basis of Disease Center

Institute for Dementia Research & Prevention

Louisiana Clinical & Translational Science Center

Nutrition Obesity Research Center

Metamor Institute

Center for Military Performance & Resilience

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Human Research Protections Program

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6400 Perkins Rd.
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