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Clinical Research Data Abstractor Jobs in Baton Rouge, LA

Womans

Scientific Research Director

Baton Rouge, LA · On-site

$102.13 - $151.92/hr

Experience in study design, data collection, data quality control, research execution, grant ... Supports a high-paced, high-volume research program conducting clinical and epidemiological women ...

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All JobsClinical Research Data Abstractor JobsClinical Research Data Abstractor Jobs in Baton Rouge, LA

Clinical Research Data Abstractor information

See Baton Rouge, LA salary details

$17

$42

$60

How much do clinical research data abstractor jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for clinical research data abstractor 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 the difference between Clinical Research Data Abstractor vs Clinical Research Coordinator?

AspectClinical Research Data AbstractorClinical Research Coordinator
Primary RoleExtracts and summarizes data from clinical trial recordsManages overall study operations and participant coordination
Required SkillsAttention to detail, data management, basic medical knowledgeRegulatory compliance, patient interaction, study oversight
Work EnvironmentData entry labs, clinical trial sites, research officesClinical sites, hospitals, research institutions
CertificationsTypically none required, but certifications like CCR can helpOften requires CCRC or similar certifications

While both roles support clinical research, the Clinical Research Data Abstractor focuses on data extraction and analysis, whereas the Clinical Research Coordinator manages study logistics and participant interactions. Understanding these differences helps in choosing the right career path or job search focus.

What are common challenges faced by clinical research data abstractors, and how can they be managed?

Clinical Research Data Abstractors often encounter challenges such as interpreting complex medical records, ensuring data accuracy, and navigating various electronic health record (EHR) systems. To manage these challenges, it's helpful to develop strong attention to detail, maintain up-to-date knowledge of medical terminology, and collaborate closely with clinical teams for clarification when needed. Additionally, frequent communication with data managers and adhering to standardized data abstraction protocols can greatly reduce errors and improve data quality.

What is a clinical research data abstractor?

A Clinical Research Data Abstractor is a professional responsible for collecting and extracting important data from medical records, clinical trials, or patient charts. They ensure that the data is accurate, complete, and entered into research databases or electronic systems. This role is vital in supporting clinical research studies by ensuring high-quality data for analysis, compliance, and reporting. Clinical Research Data Abstractors often work closely with research coordinators, physicians, and other healthcare professionals.

What skills and qualifications are needed to be a clinical research data abstractor?

To thrive as a Clinical Research Data Abstractor, you need strong attention to detail, knowledge of medical terminology, and experience with data collection, often supported by a degree in health sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and possibly certifications like ACRP-CP or SoCRA-CCRP is common. Excellent organizational skills, critical thinking, and the ability to communicate clearly with research teams help set top performers apart. These skills ensure accurate, timely data abstraction that is vital for regulatory compliance and the integrity of clinical research studies.
What are popular job titles related to Clinical Research Data Abstractor jobs in Baton Rouge, LA? For Clinical Research Data Abstractor jobs in Baton Rouge, LA, the most frequently searched job titles are:
What job categories do people searching Clinical Research Data Abstractor jobs in Baton Rouge, LA look for? The top searched job categories for Clinical Research Data Abstractor jobs in Baton Rouge, LA are:
What cities near Baton Rouge, LA are hiring for Clinical Research Data Abstractor jobs? Cities near Baton Rouge, LA with the most Clinical Research Data Abstractor job openings:
Clinical Research Data Abstractor jobs near you
Infographic showing various Clinical Research Data Abstractor job openings in Baton Rouge, LA as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $88,147 per year, or $42.4 per hour.

Clinical Research Data & Regulatory Coordinator

Mary Bird Perkins Cancer Center

Baton Rouge, LA • On-site

$23.25 - $31/hr

Full-time

Posted 22 days ago

Mary Bird Perkins Cancer Center rating

7.6

Company rating: 7.6 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

Job description

Mary Bird Perkins Cancer Center is Louisiana's leading cancer care organization, caring for more patients each year than any other facility in the region. And with strategic hospital and physician partnerships, we are delivering on our mission to improve survivorship and lessen the burden of cancer.

Mary Bird Perkins and its partners work together to provide state-of-the-art treatments and unparalleled collaborative, comprehensive cancer services. This culture of innovation helps attract the best cancer minds in the country, from expert physicians and highly specialized scientists to forward-thinking leaders in supportive care and other disciplines.

Together, with our hospital and physician partners, we are one-hundred percent focused on cancer care.

Why Join Us? We are looking for talented and highly-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.

Job Description:

100% IN PERSON POSITION

SCOPE:The Data and Regulatory Coordinator collaborates with the Clinical Research team and the Principal Investigator by knowledge of current protocol requirements; maintains IRB documents, regulatory and protocol documentation for assigned clinical trials administered by the Center which may include multi-site trials; facilitates communication and correspondence between Clinical Research and sponsoring agencies; collects protocol specific information from physicians, nurses, patients, family members, local caregivers, and others utilizing protocol specific methods; ensures that all designated Clinical Research regulatory and data management activities for all clinical research sites are executed in accordance with all applicable laws, regulations, policies and protocol requirements; performs additional duties as requested by supervisor and/or described in position description.

ESSENTIAL FUNCTIONS:

1. Demonstrates knowledge and understanding of the evolution of clinical research.

2. Participates in clinical research studies by assuring that the regulatory and data for trials being managed according to rules and guidelines governing the conduct of clinical research trials.

3. Monitor/Auditor Preparation and Participation

4. IRB Preparation and Presentation

5. Protocol research document maintenance

6. Policies & procedures

7. Other duties and professional development

QUALIFICATIONS:

  • Bachelor's degree or equivalent work experience, preferably in a scientific or technical discipline.

  • Basic science degree, or certification or licensure in a health care field

  • Demonstrated success in management of regulatory submissions activities.

  • Medical or scientific research experience preferred.

  • Professional Certifications preferred

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