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Source Inspector Jobs in Arkansas (NOW HIRING)

Pepper Source

RO Quality Control - 3rd Shift

Rogers, AR · On-site

$18.50/hr

Job Type Full-time Description Job Title: Quality Control Reports To: Department Supervisor FLSA Status: Hourly Non-Exempt 3rd Shift Hours: 10:30pm-7:00am Overtime required based on production needs.

PH FM LLC

Field Operations Manager

Little Rock, AR

Quality Service Inspectors would also be in your market doing inspections so that all sites are ... You would be responsible for hiring Contract Partners for relinking sites and help source Contract ...

PHFM

Field Operations Manager

Little Rock, AR · On-site

Quality Service Inspectors would also be in your market doing inspections so that all sites are ... You would be responsible for hiring Contract Partners for relinking sites and help source Contract ...

PH FM LLC

Field Operations Manager

Little Rock, AR · On-site

Quality Service Inspectors would also be in your market doing inspections so that all sites are ... You would be responsible for hiring Contract Partners for relinking sites and help source Contract ...

SeaWorld

Safety Specialist, Senior

Busch, AR · On-site

$15/hr

Complete daily, weekly and monthly regulatory inspections of the hazardous waste facility, collection sites, UST/AST, oil/grease containers, generators and any other potential pollution source ...

Chloeta

Geotechnical Engineer

Little Rock, AR · On-site +1

... inspection, environmental coordination, and technical analysis for new construction, renovations ... material source characterization; landslide analyses and mitigation recommendations ...

Alter Trading Corp

Mechanic

North Little Rock, AR · On-site

Alter is committed to our customers by being the best source of both ferrous and non-ferrous metal ... Inspect and conduct preventive maintenance on all equipment 2. May maintain facility equipment, on ...

Signal Energy

Quality Manager

Lake Village, AR · On-site

Director of Quality Supervises: QA/QC Inspectors Works closely with: Project Engineer, Project ... through this source. In addition, Signal Energy Constructors or its affiliates will not be ...

Applied High Voltage

Quality Manager

Lake Village, AR · On-site

Director of Quality Supervises: QA/QC Inspectors Works closely with: Project Engineer, Project ... through this source. In addition, Signal Energy Constructors or its affiliates will not be ...

Applied High Voltage

Quality Manager

Lake Village, AR · On-site

Director of Quality Supervises: QA/QC Inspectors Works closely with: Project Engineer, Project ... through this source. In addition, Signal Energy Constructors or its affiliates will not be ...

Signal Energy

Quality Manager

Lake Village, AR · On-site

Director of Quality Supervises: QA/QC Inspectors Works closely with: Project Engineer, Project ... through this source. In addition, Signal Energy Constructors or its affiliates will not be ...

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Showing results 21-40

All JobsSource Inspector JobsSource Inspector Jobs in Arkansas

Source Inspector information

See Arkansas salary details

$7

$18

$28

How much do source inspector jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for source inspector in Arkansas is $18.55, according to ZipRecruiter salary data. Most workers in this role earn between $14.90 and $20.29 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a source inspector, and why are they important?

To thrive as a Source Inspector, you need a solid understanding of quality control standards, inspection procedures, and relevant industry regulations, often supported by a technical degree or certification such as ASQ Certified Quality Inspector. Familiarity with measurement tools, inspection software, and documentation systems is typically required. Attention to detail, strong analytical thinking, and effective communication are critical soft skills for ensuring accurate assessments and clear reporting. These skills and qualifications are essential for maintaining product quality, meeting client specifications, and supporting supplier compliance.

What does a source inspector do?

As a source inspector, you act as a field representative for a manufacturing company. Your duties involve inspecting materials and components at the facility that produces them. You work to ensure that parts meet their required specifications, and you do this by looking at blueprints and data. Other responsibilities include taking measurements, performing tests using computer equipment or electrical devices, and assessing other variables such as density, strength, and durability. You document the results of these inspections and create a report for your client or employer. Many source inspectors work in the aerospace industry.

How does a source inspector typically collaborate with suppliers and internal quality teams during the inspection process?

Source Inspectors work closely with suppliers to verify that products and components meet specified quality standards before shipment. They coordinate with internal quality assurance teams to ensure that inspection criteria align with company and industry requirements. Effective communication and documentation are essential, as Source Inspectors often discuss findings, resolve discrepancies, and provide feedback to both the supplier and their own organization. This collaborative approach helps prevent costly quality issues downstream and fosters strong supplier relationships.

What is the difference between Source Inspector vs Quality Control Inspector?

AspectSource InspectorQuality Control Inspector
CertificationsTypically requires NDT certifications, inspection licensesOften requires quality assurance certifications, such as ASQ certifications
Work EnvironmentPrimarily on-site at manufacturing or construction sites, inspecting materials and componentsWorks in manufacturing facilities, labs, or on-site, focusing on product quality
Industry UsageCommon in construction, manufacturing, and oil & gas industriesWidely used across manufacturing, aerospace, automotive, and industrial sectors

Source Inspectors focus on verifying the origin and compliance of materials and components, often requiring specialized certifications. Quality Control Inspectors concentrate on ensuring finished products meet quality standards. While both roles involve inspection, their scope and focus differ based on the stage of production and specific industry requirements.

More about Source Inspector jobs
What are popular job titles related to Source Inspector jobs in Arkansas? For Source Inspector jobs in Arkansas, the most frequently searched job titles are:
What job categories do people searching Source Inspector jobs in Arkansas look for? The top searched job categories for Source Inspector jobs in Arkansas are:
What are popular job titles related to Source Inspector jobs in AR? For Source Inspector jobs in AR, the most frequently searched job titles are:
Source Inspector jobs near you
Infographic showing various Source Inspector job openings in Arkansas as of August 2026, with employment types broken down into 85% Full Time, 11% Part Time, and 4% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $38,578 per year, or $18.5 per hour.

Clinical Research Coordinator

American Oncology Network

Hot Springs, AR • On-site

$53K - $93K/yr

Full-time

Posted 24 days ago

American Oncology Network rating

6.7

Company rating: 6.7 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

533rd of 887 rated healthcare providers

Job description

Location:
Genesis Cancer and Blood Institute
Pay Range:
$53,040.00 - $93,267.20
Position Summary
The Clinical Research Coordinator functions as an integral part of the Research Team in clinical trial management at Oncology Consultants. The Clinical Research Coordinator is involved in multiple aspects of the research process under the general supervision of the Clinical Research Manager and the Research Director.
Key Performance Areas
KPA 1 - Study Start-Up, Regulatory & Site Initiation
Responsible for supporting study feasibility, regulatory submissions, and study initiation activities to ensure compliance with protocols, regulatory requirements, and institutional policies.
  • Applies knowledge of study design to evaluate protocol feasibility at the site.
  • Assists Regulatory staff in preparing and submitting documents to Institutional Review Board (IRB).
  • Participates in study site initiation activities.
  • Attends and participates in investigator meetings and clinical trial conferences as directed.
  • Documents protocol deviations and exemptions.
  • Prepares for and participates in FDA inspections.
  • Communicates effectively with IRBs, sponsors, investigators, and research team members.

KPA 2 - Patient Recruitment, Screening & Enrollment
Responsible for patient recruitment, screening, eligibility verification, and enrollment activities in accordance with study protocols.
  • Participates in subject/patient recruitment and evaluation of eligibility.
  • Reviews and verifies required source documents to confirm study eligibility.
  • Reviews inclusion/exclusion criteria with investigator to assure subject eligibility.
  • Conducts interviews to assess subject ability and willingness to complete study procedures.
  • Maintains patient screening and enrollment logs.
  • Reviews protocol requirements, informed consent, and follow-up procedures with potential study subjects.
  • Follows randomization procedures per protocol.
  • Demonstrates commitment to superior customer service and patient-centered communication.

KPA 3 - Clinical Trial Coordination & Patient Care Activities
Responsible for coordinating study visits, performing clinical procedures, and ensuring protocol compliance throughout the research process.
  • Ensures study drugs are dispensed per protocol and maintains drug accountability records.
  • Reviews returned drugs for compliance and documents findings.
  • Provides direct care in study compliance throughout the research experience.
  • Performs peripheral venipuncture per organizational standards.
  • Ensures proper specimen collection, batching, processing, and shipping per protocol.
  • Works collaboratively with site staff to process specimens.
  • Prepares and ships study-required specimens per protocol manual.
  • Obtains test results and reports to the physician investigator.
  • Attends clinic visits with the investigator and assists in following study guidelines.

KPA 4 - Data Management, Documentation & Monitoring Support
Responsible for maintaining accurate study documentation, source documentation, and supporting sponsor monitoring and audit activities.
  • Obtains and reviews original source documents (recordings, scans, test results, procedure reports).
  • Abstracts data from medical records and other documentation to study forms and flow sheets.
  • Completes and maintains study documentation and case report forms.
  • Resolves data queries.
  • Schedules sponsor monitoring visits.
  • Prepares case report forms and source documents for sponsor and audit review.
  • Assists with audit preparation and monitoring visits.

KPA 5 - Research Program Support, Education & Administrative Support
Responsible for supporting research department operations, education, budgeting support, and departmental coordination activities.
  • Participates in educational and training activities and continuing education.
  • Supports and assists management team with department projects.
  • Assists in maintenance of budgetary data for each clinical trial.
  • Assists in planning department coverage for clinic visits, data management, and meetings.
  • Maintains professional communication with internal and external customers.
  • Demonstrates strong verbal and written communication skills.

Position Qualifications
Education
  • Degree in the life sciences or health sciences such as Registered Nurse (R.N.), Doctor in Philosophy (Ph.D.), Medical Doctorate (M.D.), or other related degree.

Minimum Relevant Experience
  • 2 or more years of clinical research experience.

Certifications/Licenses
  • Continuing education participation is expected, and research certification through a recognized national organization (SOCRA, ACRP) is encouraged.
  • NIH protection of Human subjects online course will be required annually.
  • IATA training will be required every 2 years.

Travel: 0 - 25%
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