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Non Exempt Image Data Entry Jobs in Myrtle Beach, SC

Spray Technician

Myrtle Beach, SC · On-site

$15.50 - $19.75/hr

Non-Exempt The Spray Technician is responsible for all phases of the management of truck operations ... Maintains clean, neat and professional image of service vehicle & equipment Equipment Management

Non-Essential Functions: Perform all other tasks as assigned. Qualifications and Desired Skills ... Data entry. * 80% of the time sitting. * Some bending/stooping. * Lifting less than 35lbs.

Non-Essential Functions: Perform all other tasks as assigned. Qualifications and Desired Skills ... Data entry. * 80% of the time sitting. * Some bending/stooping. * Lifting less than 35lbs.

Non-Essential Functions: Perform all other tasks as assigned. Qualifications and Desired Skills ... Data entry. * 80% of the time sitting. * Some bending/stooping. * Lifting less than 35lbs.

Phlebotomist

Conway, SC · On-site

$22.81 - $24.45/hr

Demonstrates organizational commitment and promotes a positive image to patients, clients ... Keyboard/data entry experience. * Shift/Time Zone: Day/EST Candidate will be required to do ...

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Non Exempt Image Data Entry information

See Myrtle Beach, SC salary details

$9

$17

$25

How much do non exempt image data entry jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for non exempt image data entry in Myrtle Beach, SC is $17.53, according to ZipRecruiter salary data. Most workers in this role earn between $14.71 and $19.66 per hour, depending on experience, location, and employer.

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Cities near Myrtle Beach, SC with the most Non Exempt Image Data Entry job openings:

Infographic showing various Non Exempt Image Data Entry job openings in Myrtle Beach, SC as of August 2026, with employment types broken down into 69% Full Time, and 31% Part Time. Highlights an 100% In-person job distribution, with an average salary of $36,453 per year, or $17.5 per hour.

Clinical Research Assistant

Headlands Research

Myrtle Beach, SC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago


Job description

Clinical Research Assistant (non-lab)

 Location: Myrtle Beach, SC  | Site Name: Trial Management Associates - Myrtle Beach  | Full-Time  | Clinical Research

We're seeking a Clinical Research Assistant (RA) for our clinical research site located in Myrtle Beach, SC. As an RA, you won't just be supporting research-you'll be helping shape the future of healthcare. This is an exciting opportunity for individuals with clinical experience who are ready to grow their skillset and income potential within the clinical research field.

The Role:

As a Clinical Research Assistant, you'll work side-by-side with experienced Clinical Research Coordinators, Investigators, and cross-functional teams to support all aspects of clinical trial execution-from subject screening to data entry. Your work will directly contribute to the success of new treatments in development.

Type:  Regular Full-time Employee
Schedule:  Mondays through Thursdays 7:00am - 4:30pm, and Fridays 7:30am - 11:30am
Location:  Onsite in Myrtle Beach, SC (no capabilities for remote or hybrid work)
Reports to:  Site Lead
Benefits:  Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

What We Offer
  • Competitive pay + annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays
  • Opportunities for professional development and career growth
  • A mission-driven culture focused on advancing medicine and improving patient outcomes

Responsibilities:

  • Assist research coordinators in conducting clinical trial visits in compliance with study protocols
  • Collect and record vital signs, make study-related phone calls, and document data in electronic systems
  • Support subject screening, enrollment, and follow-up processes
  • Review and verify study documentation for accuracy and completeness
  • Maintain close communication with coordinators, investigators, and study participants

Requirements:

  • Familiarity with medical terminology required
  • Prior experience providing direct hands-on patient care required
  • Clinical research experience preferred
  • Comfortable using multiple electronic data entry systems
  • Strong attention to detail, time management, and ability to work in a fast-paced, regulated environment
  • Excellent interpersonal skills-you'll be interacting with participants, providers, and sponsors
  • Passion for improving patient outcomes through research