ZipRecruiter

Log In

1

Clinical Data Associate Jobs in Arkansas (NOW HIRING)

L3HHCM20

Senior Associate, Quality Engineer

Camden, AR · On-site

$75K - $101K/yr

Senior Associate, Quality Engineer Job Code: 40606 Job Location: Camden, Arkansas Job Schedule: 4 ... systems, field and clinical data. Further investigates the cause for discrepancies and ...

Ohio State University

Clinical Research Associate (CRA) Position Summary The Clinical Research Associate (CRA) will ... Perform routine data quality checks and resolve queries in a timely manner * Ensure accurate and ...

next page

Showing results 1-20

All JobsClinical Data Associate JobsClinical Data Associate Jobs in Arkansas

Clinical Data Associate information

See Arkansas salary details

$11

$32

$71

How much do clinical data associate jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for clinical data associate in Arkansas is $32.21, according to ZipRecruiter salary data. Most workers in this role earn between $24.23 and $32.21 per hour, depending on experience, location, and employer.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

What are the key skills and qualifications needed to thrive as a clinical data associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

What is the difference between Clinical Data Associate vs Clinical Research Coordinator?

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

More about Clinical Data Associate jobs
What are the most commonly searched types of Clinical Data jobs in Arkansas? The most popular types of Clinical Data jobs in Arkansas are:
What are popular job titles related to Clinical Data Associate jobs in Arkansas? For Clinical Data Associate jobs in Arkansas, the most frequently searched job titles are:
What job categories do people searching Clinical Data Associate jobs in Arkansas look for? The top searched job categories for Clinical Data Associate jobs in Arkansas are:
What cities in Arkansas are hiring for Clinical Data Associate jobs? Cities in Arkansas with the most Clinical Data Associate job openings:
Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Arkansas as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $66,996 per year, or $32.2 per hour.

Senior Associate, Quality Engineer

L3HHCM20

Camden, AR

Full-time

Re-posted 27 days ago

Job description

Job Title: Senior Associate, Quality Engineer

Job Code: 40619

Job Location: Camden, Arkansas

Job Schedule:  4/10 First shift, Employees work 10 hour days, 4 days a week

Job Description:

L3Harris Technologies is seeking a Specialist, Quality Engineer to join our growing facility in Camden, Arkansas.  This role will be responsible for the design, development and implementation of standards, methods and procedures for inspecting, testing and evaluating the precision and accuracy of company products in compliance with contractual and regulatory requirements. Performs analysis on reported nonconformities and discrepancies related to assembly, process, mechanical, electrical, electro-mechanical systems, field and clinical data. The individual further investigates the cause for discrepancies and nonconformities to develop disposition and recommend corrective action plans. Leads material review board and Process Failure Mode Effects Analysis (PFMEA) activities. Interfaces with manufacturing, engineering, customer, vendor and subcontractor representatives to ensure requirements are met. Conducts program quality cost account management and manages supplier corrective actions. Serves as the primary interface to customers and supplier for quality related matters.

Essential Functions:

  • Ensure program design and process documents for area of responsibility include program quality requirements and that products are inspectable.
  • Independently reviews manufacturing planning to ensure appropriate design engineering requirements implementation, material traceability maintenance, quality record maintenance and operator and inspector sign-offs: Designates inspection/verification needs.
  • Process Failure Modes and Effects Analysis (PFMEA): Leads effort to quantify and reduce risk using this quality tool. 
  • Actively participates in improvement teams to reduce risk through the application of mistake proofing principles.
  • Inspects method development and implementation: Develops, implements and monitors new or existing inspection methods to ensure products meet stated engineering requirements.
  • Ensures compliance to all quality system requirements through a thorough knowledge of documented requirements.
  • Independently conducts process audits to ensure processes are following manufacturing planning, program requirements and enterprise level command media.
  • First Article Inspection execution per AS9102 requirements. 
  • Performs documentation reviews in support of hardware acceptance (HAR) activities. Develops and maintains Quality Documentation Control Center QDCC command media. Monitors manufacturing schedules and QDCC activities in support of HAR customer HAR requirements. Creates Acceptance Data Packages - ADP in support of hardware selloff.
  • Actively participates in the Material Review Board, including segregation and control of nonconforming hardware to preclude inadvertent processing, disposition nonconforming hardware, preparing for and conducting board meetings, and implementing disposition decisions.
  • Drives corrective and preventive action to ensure continual improvement: Investigates and determines root causes of problems, develops and implements corrective and preventive actions.
  • Provides imaginative, thorough and practical solutions to a wide range of technical problems through the application of quality engineering disciplines and tools.
  • Ability to obtain a US Secret Security Clearance.
  • Ability to travel less than 10%.

Qualifications:

  • Bachelor's Degree and a minimum of 2 years of prior related experience. Graduate Degree or equivalent with 0 to 2 years of prior related experience. In lieu of a degree, minimum of 6 years of prior related experience 

Preferred Additional Skills:

  • Computer skills sufficient to generate reports and analyze data using MS Excel, MS PowerPoint, and MS Word software. PowerBi is a plus. 
  • Experience with solid rocket component fabrication, electro-mechanical parts assembly and Final Assembly and Check-out and/or Avionics.
  • Experience with Hardware Acceptance Review processes.
  • ASQ certification a plus.
  • Experience implementing cost-effective, LEAN inspection/verification methods or Key Characteristics (ref AS9103).

#LI-NA87 

Apply