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Clinical Research Data Abstractor Jobs in Monroe, LA

FMOLHS

RN - Cardiology Clinic

Monroe, LA · On-site

May serve as preceptor for clinical staff. Relies on experience and judgment to accomplish ... Patient psychosocial/physiologic assessments that integrates changing data are performed at all ...

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All JobsClinical Research Data Abstractor JobsClinical Research Data Abstractor Jobs in Monroe, LA

Clinical Research Data Abstractor information

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$17

$42

$60

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

As of Aug 30, 2026, the average hourly pay for clinical research data abstractor in Monroe, LA is $42.45, according to ZipRecruiter salary data. Most workers in this role earn between $34.90 and $50.38 per hour, depending on experience, location, and employer.

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 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 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 job categories do people searching Clinical Research Data Abstractor jobs in Monroe, LA look for?

The top searched job categories for Clinical Research Data Abstractor jobs in Monroe, LA are:

What cities near Monroe, LA are hiring for Clinical Research Data Abstractor jobs?

Cities near Monroe, 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 Monroe, LA as of June 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $88,303 per year, or $42.5 per hour.

Clinical Research Coordinator- Monroe, LA

Monroe, LA • On-site

Welcome - The IMA Group
See more jobs at Welcome - The IMA Groupexternal

$23.25 - $31/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 4 days ago

Job description

Clinical Research Coordinator (CRC) - Monroe, LAAdvance Your Career While Advancing Medicine

Are you an experienced Clinical Research Coordinator looking to make a meaningful impact? Join IMA Clinical Research in Monroe, LA, where you'll help bring innovative treatments to patients through cutting-edge clinical trials.

As a Clinical Research Coordinator, you'll lead the day-to-day management of industry-sponsored clinical research studies, working alongside physicians, sponsors, and research professionals to ensure every study is conducted with the highest standards of quality, safety, and regulatory compliance. If you're organized, patient-focused, and thrive in a fast-paced environment, we'd love to hear from you.

What You'll Do

  • Coordinate all phases of clinical trials from study start-up through closeout.
  • Perform phlebotomy and collect study-related samples and data.
  • Ensure compliance with FDA, ICH-GCP, sponsor protocols, and site SOPs.
  • Educate and support study participants throughout their research journey.
  • Collaborate with investigators, sponsors, CROs, IRBs, and laboratory partners.
  • Maintain accurate source documentation and report adverse events as required.

What You'll Bring

  • 2+ years of Clinical Research Coordinator experience
  • Phlebotomy experience required
  • Experience with industry-sponsored investigational product (IP) studies required
  • Bachelor's degree required; CCRC certification preferred
  • Excellent organizational, communication, and problem-solving skills

Why Join IMA Clinical Research?

  • Competitive compensation
  • Medical, Dental & Vision Insurance
  • 401(k) with Company Match
  • Generous PTO, Paid Holidays & Floating Holiday
  • Tuition Reimbursement & Student Loan Repayment Assistance
  • Paid Parental Leave
  • Company-paid Life, Short-Term & Long-Term Disability Insurance

Join a collaborative team that's committed to improving lives through clinical research. If you're ready to grow your career while helping shape the future of medicine, we encourage you to apply today.

The IMA Group is an Affirmative Action/Equal Opportunity Employer

Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.

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Employment Type: Full-Time

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