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Clinical Research Assistant Jobs in Baton Rouge, LA

Louisiana State University

Transient

Baton Rouge, LA · On-site

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

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$44

How much do clinical research assistant jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical research assistant in Baton Rouge, LA is $21.81, according to ZipRecruiter salary data. Most workers in this role earn between $16.63 and $24.95 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.
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Clinical Research Assistant jobs near you
Infographic showing various Clinical Research Assistant job openings in Baton Rouge, LA as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 16% Part Time, 2% Temporary, and 6% Contract. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $45,362 per year, or $21.8 per hour.

Clinical Research Assistant - OLOL

FMOLHS

Baton Rouge, LA • On-site

Full-time

Posted 4 days ago

Key responsibilities

  • Coordinate and implement assigned research study activities, including recruitment, screening, and enrollment of patients.

  • Collect, enter, and manage clinical data, ensuring accuracy and compliance with protocol requirements.

  • Communicate with research team members, participants, and sponsors regarding protocol activities, adverse events, and study updates.

Job description

Under the direct supervision of the Clinical Research Manager and the Principal Investigator (PI), the Research Assistant is responsible for the coordination and implementation of assigned research projects, data management, and communication of protocol activity within the Office of Research.

Our Lady of the Lake Health provides care for a full range of illness or injury, including those that are extremely complex, for both pediatric and adult patients. We are a nonprofit, Catholic healthcare ministry based in Baton Rouge with more than 7,500 employees and more than 2,900 active physicians, including more than 600 employed physicians.

We are committed to building a healthy community through excellence in patient care and education. Being our best earns us the trust and loyalty of our community, and our culture of excellence is directly tied to our mission. We believe in the value of receiving a broad range of healthcare from one trusted provider, and we pursue and provide a comprehensive range of advanced programs, treatments and technologies.

  • 5 years research or healthcare related experience may be substituted for a Bachelor's degree.
  • Bachelor's Degree
  • Software applications, databases, spreadsheets, and word processing required. Excellent organizational skills required. Excellent attention to detail skills required. Must have ability to manage multiple and competing priorities. Must have oral and written communication skills. Must be able to work independently. Must be able to work with other professionals
  1. Coordination and Implementation of Study Activities
    1. Conducts recruitment, screening and enrolling of eligible patients into clinical trials.
    2. Explains protocol in detail and conducts informed consent procedure with potential research participants as deemed appropriate by the clinical research manager.
    3. Assists Clinical Research Manager to prepare for site visits and study initiation.
    4. Maintains complete working knowledge of all assigned protocols and reporting requirements.
    5. Maintains study-specific supplies and equipment.
    6. Collects study specimens according to protocol, processing, and preparation for shipping.
    7. Attends study meetings as requested by Clinical Research Manager and/or PI.
    8. Collaborates with Clinical Research Nurse and PI to manage study activities.
  2. Data Management
    1. Collects, enters, and compiles clinical data required by protocol ensuring accuracy and timeliness of data entry.
    2. Maintains study files pertaining to clinical trials and completes source documents/case report forms.
  3. Communication
    1. Communicates with Clinical Research Manager, PI, subjects, sponsor and other clinical trial personnel in a timely, efficient, and comprehensive manner.
    2. Communicates any adverse event, or protocol deviation to Clinical Research Manager and documents appropriately.
    3. Coordinates with Clinical Research Manager to identify procedures, laboratory tests, and protocol events that require consideration for financial, legal, and regulatory compliance.
    4. Collaborates with PI and Clinical Research Manager to develop materials and tools necessary to appropriately train key personnel in the protocol requirements, schedule of visits, and execution of clinical trial agreement.
  4. Other Duties As Assigned
    1. Performs other duties as assigned or requested.

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