Clinical Research Coordinator Jobs in Arkansas
Clinical Research Coordinator jobs in Arkansas are concentrated in Little Rock and Fayetteville, where major employers like UAMS (University of Arkansas for Medical Sciences), Arkansas Children's Hospital, and Walmart-affiliated health initiatives anchor most of the hiring activity. Demand is strongest in oncology, cardiovascular, and Phase II-IV pharmaceutical trials, with openings at every level from entry-level research assistant to senior coordinator managing multi-site studies. The market is steady and driven by UAMS's role as the state's only academic medical center with an active clinical trials portfolio. See the openings below and apply to the ones that match your experience.
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At the heart of innovative cancer research is compassionate, expert patient care. We are seeking a Research Financial Analyst who is passionate about overseeing the cash flow of clinical trials while helping bring tomorrow's cancer therapies to patients today.
Highlands Oncology began in 1996 with three physicians and a desire to change the face of oncology care in our community. Dr. Malcolm Hayward, Dr. Dan Bradford, and Dr. Thad Beck knew that patients do better at home, in the community where they live and work, and where their support system is already in place. In furthering that goal, Highlands has grown with the region from a single location 30 years ago, to 6 locations in Northwest and Northcentral Arkansas today employing more that 850 diverse team members.
As Northwest Arkansas continues to grow, so must the services and providers available in the region. Highlands Oncology is committed to remaining on the cutting edge to ensure our community has access to there very best cancer care. What we have is something quite unique right here in our own backyard with a caring multidisciplinary team focused on treating patients like family.
Highlands Oncology research department has provided clinical trials to our community for over 30 years, including many first-in-human cancer treatments. Our department is committed to remaining on the cutting edge to ensure our community has access to many clinical trial opportunities. We have worked with the pharmaceutical industry to develop many treatments that are standard practice today.
Job Summary:
The Research Financial Analyst manages end to end invoicing and patient reimbursements, The role conducts ongoing reconciliation of sponsor payments, study expenses, and CTMS financial data, resolving discrepancies, and maintaining audit ready documentation. The analyst oversees expense management and coordinates with Accounts Payable. They provide advanced CTMS management. The position collaborates with all Research and Highlands teams, as well as external partners such as pharmaceutical sponsors and healthcare entities, while adhering to FDA regulations, Good Clinical Practice, Highlands Oncology policies, and sponsor requirements.
Job Duties / Responsibilities:
Invoice & Reimbursement Management
Process, review, and issue accurate patient and sponsor invoices in alignment with study budgets and contract terms; coordinate patient reimbursement workflows, maintain required documentation, and manage inventory of Highlands payment cards and sponsor provided reimbursement cards.
Billing Accuracy & Financial Coordination — Validate study related activities to ensure all billable items are captured and correct; work with the Highlands Oncology Business Office to ensure patient reimbursements are paid.
Communication & Audit Readiness — Collaborate with clinical and data teams and Sponsors to resolve invoice discrepancies and maintain transparent financial tracking; maintain complete, audit ready financial documentation for internal reviews and sponsor audits.
Reconciliation
Account Reconciliation — Perform reconciliation of sponsor payments, patient reimbursements, and study-related expenses against Study Contract and Budget and CTMS data.
Variance Analysis — Identified, investigated, and resolved financial variances, ensuring alignment between site records, sponsor remittances, and contractual budgets.
Payment Tracking — Monitored incoming sponsor payments, applied funds to correct studies/visits in CTMS, and escalated overdue or missing payments.
Expenses
Expense Oversight & Budget Management — Track, categorize, and monitor department and grant/clinical trial expenditures; develop and maintain the annual department budget; prepare short and long term financial forecasts and revenue/expense analyses to support strategic planning and decision making.
Compliance Review & AP Coordination — Verify invoices and supporting documentation for accuracy and compliance with institutional and sponsor contracts; ensure all approved invoices are submitted to Accounts Payable and processed for timely payment.
Reporting & Budget Monitoring — Prepare detailed monthly and quarterly expense reports; monitor budgets to flag overspend risks and expense anomalies to Supervisor.
Clinical Trial Management System (CTMS) Management
CTMS Configuration & Study Setup — Oversee CTMS setup by building study calendars, creating milestones, and configuring invoiceable items. Ensure that configurations are aligned with study budgets, visit schedules, and contract terms.
Data Integrity & System Reporting — Maintain accurate, up to date CTMS data by validating visit completions, milestones, budgets, and payment schedules; generate financial reports, dashboards, and study performance metrics for internal and sponsor use.
Workflow Management & Cross Functional Support — Manage CTMS workflows, update statuses, troubleshoot system issues, and collaborate with clinical and data teams to ensure CTMS data reflects real world study progress.
Demonstrate a high level of professionalism and responsiveness when interacting with internal and external customers and patients.
Demonstrates effective oral and written communication skills.
Attends required research department meetings/activities.
Maintain patient/sponsor confidentiality.
Promptly report to work at designated times and maintain good attendance with no unexcused absences.
Support and adhere to organizational decisions, policies, and procedures.
Willingly accept assignments and complete them in a timely manner and cross train and provide back-up as needed.
Required Skills/Abilities:
Ability to gather reasonable retrievable information to organize and perform financial analysis assignments.
Advanced skills in using spreadsheets and database software in financial analysis, fiscal management, and financial reports.
Ability to manage high volume and complex transactions.
Ability to perform complex financial analysis and customized reporting.
Proficient in computer skills including Microsoft Office: Outlook, Word, Excel.
Maintain continuing education hours as required.
Maintain all licenses, certifications, and qualifications as required.
Certifications/Licenses/Education/or Experience in a related field:
Bachelor’s degree in business (Auditing, Finance, Accounting), or Healthcare Administration, or high school diploma or GED plus 3 years of related experience in lieu of bachelor’s degree.
1+ years of experience in medical billing, research, or oncology preferred.
Experience in preparing, managing, and projecting budgets.
Knowledge of finance policies, practices, and systems.
Experience with all types of reward mechanisms, including grants, contracts, clinical trials, subcontracts, and cooperative agreements preferred.
Must complete registration with ID.me upon hire.
Clinical Research Professional (CCRP, CCRC, CCRA, or equivalent) certification preferred (within three years of hire)
Physical Requirements:
May be asked to lift up to 25 pounds. Lifting could include binders, reams of paper, and office supplies.
Will require extensive desk and computer use.
Work Environment:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of the job. Reasonable accommodation may be made to enable individuals with disabilities to perform essential functions.
Due to the nature of our business and the use of radiation and hazardous chemicals, it is imperative that all employees foster a culture and environment of safety.
Safety Sensitive: In accordance with Arkansas code this position is designated as a safety sensitive position wherein the employee performing the job duties under the influence may constitute a threat to health or safety.
Highlands Oncology offers a full suite of benefits that includes those pictured below and MANY MORE...
- Certified a Great Place to Work!
See All 27 Clinical Research Coordinator Jobs in Arkansas
Find roles in Arkansas that match your experience and apply in just a few clicks.
Find JobsClinical Research Coordinator Jobs by City in Arkansas
Where Arkansas roles are concentrated, by current openings.
Clinical Research Coordinator Job Market in Arkansas
A snapshot from current Arkansas openings, updated as new roles post.
Who's Hiring
- University of Arkansas7

- Walmart4

- Arkansas Children's2

- Highlands Oncology2

- 3D Imaging13
Top Industries Hiring
- Education6
- Retail4
- Healthcare & Medical Services2
- Food & Beverage1
What Arkansas Employers Look For
The qualifications that appear most often in clinical research coordinator jobs across Arkansas.
- Bachelor's degree in life sciences, nursing, or a related healthcare field required
- ACRP or SOCRA certification (CCRC or CCRP) strongly preferred or required
- Minimum one to two years of experience coordinating clinical trials preferred
- Proficiency with electronic data capture systems such as REDCap or Medidata Rave
- Demonstrated knowledge of ICH-GCP guidelines and FDA regulatory requirements
- Strong organizational skills managing IRB submissions, informed consent, and data collection
Clinical Research Coordinator Jobs in Arkansas: Frequently Asked Questions
How do you become a clinical research coordinator in Arkansas?
Most clinical research coordinator roles in Arkansas require at least a bachelor's degree in a life science, nursing, or health-related field, and employers like UAMS and Arkansas Children's Hospital typically expect applicants to hold or pursue ACRP's CCRC or SOCRA's CCRP certification. Arkansas has no state-issued license specific to clinical research coordinators, so professional certification and GCP training serve as the primary credentials. Starting in a research assistant or data coordinator role at an academic medical center or hospital-affiliated trial site is the most common entry path.
How much do clinical research coordinators make in Arkansas?
Clinical research coordinators in Arkansas earn a median of about $119,430 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $72,080 for the lowest 10% to over $226,370 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire clinical research coordinators in Arkansas?
Companies currently hiring clinical research coordinators in Arkansas include University of Arkansas, Walmart, and Arkansas Children's, per current listings on Migrate Mate as of July 2026. UAMS remains the single largest source of clinical research coordinator openings in the state given its active trials portfolio across oncology, cardiology, and rare disease research.
Which Arkansas cities have the most clinical research coordinator jobs?
Little Rock, Bentonville, and Springdale have the most clinical research coordinator openings in Arkansas. Little Rock dominates because UAMS, Arkansas Children's Hospital, and the Central Arkansas Veterans Healthcare System are all based there, while Fayetteville and Bentonville benefit from growing regional health systems and corporate wellness research tied to Walmart's health strategy in Northwest Arkansas.
Are there remote clinical research coordinator jobs in Arkansas?
Yes, but they're limited. About 10% of clinical research coordinator openings tied to Arkansas are remote or hybrid as of July 2026, reflecting that much of the role involves on-site patient contact, specimen handling, and IRB-regulated protocol tasks that cannot be done remotely. The portions most suited to remote work are regulatory document management, data entry, and sponsor or IRB correspondence.
How can I get hired as a clinical research coordinator in Arkansas with little or no experience?
The most realistic entry path is applying for a research assistant or clinical trials assistant position at UAMS or Arkansas Children's Hospital, both of which periodically post roles designed for candidates with a science degree but limited trial-specific experience. Completing a GCP certification course and gaining any IRB or patient-contact exposure through volunteer or internship work at those institutions strengthens an application considerably. Lateral moves from roles like medical assistant, phlebotomist, or clinical data abstractor are common stepping stones that Arkansas trial sites recognize as relevant.
Where can I find and apply to clinical research coordinator jobs in Arkansas?
You can find and apply to clinical research coordinator jobs in Arkansas on Migrate Mate, which lists current openings from employers across the state. Search for roles that match your experience level and specialty area, then apply directly to the ones that fit.
See All 27 Clinical Research Coordinator Jobs in Arkansas
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