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Disability Data Entry Jobs in Conway, SC (NOW HIRING)

Headlands Research

Pharmacy Coordinator

Myrtle Beach, SC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This role may also support administrative and data entry activities related to the conduct of ... of disability, accident, and life insurance options, as well as many more. What We Offer

Headlands Research

Pharmacy Coordinator

Myrtle Beach, SC

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This role may also support administrative and data entry activities related to the conduct of ... of disability, accident, and life insurance options, as well as many more. What We Offer

Mako Medical

Mobile Phlebotomist (MAKO)

Little River, SC · On-site

$16.25 - $22.25/hr

Data entry required. * Submits accurate expense forms, if applicable, on the required day ... with Disabilities This employer is required to notify all applicants of their rights pursuant to ...

Hilton Grand Vacations, Inc.

Front Desk Clerk

Myrtle Beach, SC · On-site

$12.50 - $15.50/hr

  • Retirement

  • PTO

Prior cash handling and data entry experience required When you join Hilton Grand Vacations, you ... We will ensure that individuals with disabilities are provided reasonable accommodation to ...

VOLT

Phlebotomist II

Myrtle Beach, SC · On-site

$19 - $20/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Data Entry and processing * Detail oriented and good experience. * Computer skills The ideal ... If you are an individual with a disability and need a reasonable accommodation to assist with your ...

Orscheln Industries

Applications Engineer

Conway, SC · On-site

Data entry. * 80% of the time sitting. * Some bending/stooping. * Lifting less than 35lbs ... disability, marital status, veteran status, sexual orientation, genetic information or any other ...

Orscheln Industries

Applications Engineer

Conway, SC · On-site

Data entry. * 80% of the time sitting. * Some bending/stooping. * Lifting less than 35lbs ... disability, marital status, veteran status, sexual orientation, genetic information or any other ...

Sparta Networking

Customer Service Associate

Conway, SC · On-site

$17 - $19/hr

Basic computer and data-entry skills * Ability to learn new software and procedures * Dependable ... disability, genetic information, sexual orientation, gender identity, veteran status, or any other ...

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Disability Data Entry information

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How much do disability data entry jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for disability data entry in Conway, SC is $16.61, according to ZipRecruiter salary data. Most workers in this role earn between $13.94 and $18.65 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in disability data entry, and why are they important?

To thrive as a Disability Data Entry professional, you need accurate typing skills, keen attention to detail, and a basic understanding of disability-related documentation or regulations, usually supported by a high school diploma or equivalent. Familiarity with data entry software, Microsoft Office Suite, and disability management systems such as Case Management or Claims Processing tools is often required. Strong organizational skills, discretion with confidential information, and effective communication set top performers apart. These abilities are vital to ensure data integrity, efficient processing, and compliance with privacy standards in disability services.

What is a disability data entry?

A Disability Data Entry job involves entering, updating, and managing data related to individuals with disabilities, typically for government agencies, healthcare organizations, or insurance companies. Employees in this role handle sensitive information, ensuring accuracy and confidentiality. Tasks may include processing applications, verifying documents, and maintaining compliance with legal requirements such as the ADA or HIPAA. Strong attention to detail, typing skills, and knowledge of database systems are usually required.

What does a disability data entry do?

As a Disability Data Entry specialist, your daily tasks typically include inputting and updating client or claims information, verifying data for accuracy, and maintaining electronic records related to disability services or benefits. You may also be responsible for reviewing forms for completeness, communicating with case managers or healthcare professionals to resolve discrepancies, and adhering to data privacy regulations. Collaboration with other administrative and support staff is common, especially in larger organizations. This role provides valuable insight into the administrative side of disability services and is a great foundation for broader careers in healthcare administration or case management.

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Pharmacy Coordinator

Headlands Research

Myrtle Beach, SC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago

Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.
Location: Myrtle Beach, SC | Site Name: Trial Management Associates | Full-Time | Clinical Research
Are you an experienced medical assistant or pharmacy tech looking to gain a new set of skills? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.
We're seeking a Pharmacy Coordinator for our clinical research site located in Myrtle Beach, SC. The Pharmacy Coordinator plays a key role in the successful execution of pharmaceutical clinical trials by ensuring the safe, accurate, and compliant handling of the investigational products (IP)/drug that is being studied. Working under the supervision of a licensed pharmacist or nurse (as applicable), this individual will be responsible for receiving, storing, preparing, dispensing, documenting, and managing investigational drugs in accordance with study protocols, GCP/ICH regulations, and institutional SOPs. This role may also support administrative and data entry activities related to the conduct of clinical research.
Type: Regular Full-time Employee
Schedule: Mondays through Thursdays 7:00 AM to 4:30 PM and Fridays 7:30 AM to 11:30 AM
Location: Onsite in Myrtle Beach, SC (no capabilities for remote or hybrid work)
Reports to: Site Director
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
  • A mission-driven culture focused on advancing medicine and improving patient outcomes

Why Join Us?
You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster-while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you.
Core Responsibilities:
  • Investigational Product (IP) Management
    • Receive, store, prepare, and dispense investigational products according to protocol, pharmacy manual, and regulatory requirements.
    • Use IWRS/IRT systems to log shipments, assign IP, and perform returns or destructions per study-specific guidance.
    • Maintain accurate inventory logs, temperature records, and expiration tracking for all IP and supplies.
    • Monitor and respond to temperature excursions, discrepancies, or deviations per SOP.
    • Perform aseptic preparations where required, following sterile technique protocols.
    • Manage IP accountability documentation, including blinded and unblinded logs and reconciliation.
    • Ensure all investigational product storage complies with GCP and institutional policies (double-locked, secure, labeled, etc.).
  • Documentation & Compliance
    • Maintain audit-ready records of all pharmacy activities, including temperature logs, equipment calibrations, and IP logs.
    • Create and manage pharmacy study binders with updated regulatory and protocol-specific content.
    • Adhere to ALCOA-C principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, and Consistent) in documentation practices.
    • Participate in unblinded or blinded monitoring visits, providing relevant pharmacy documentation.
  • Administrative & Operational Support
    • Assist with scheduling and performing protocol-specific assessments (e.g., memory assessments, vital signs, specimen collection support).
    • Perform data entry in eCRFs according to protocol and system-specific guidelines.
    • Support query resolution, documentation scanning, and other clerical duties (e.g., faxing, reminder calls).
    • Order pharmacy-related supplies and assist with equipment upkeep and calibrations.
    • Provide pharmacy support to other team members and backfill duties during absences.
  • Communication & Collaboration
    • Maintain clear, professional communication with study coordinators, monitors, sponsors, and clinical staff.
    • Participate in team meetings and training sessions to stay updated on protocols, SOPs, and compliance standards.
    • Demonstrate flexibility and professionalism in a fast-paced, regulated environment.

Requirements:
  • Minimum of 1-2 years of experience as a Pharmacy Technician or Medical Assistant required
  • Completion of a recognized Pharmacy Technician or Medical Assistant program
  • Registration with relevant state or provincial licensing body (e.g., College of Pharmacists of BC for Pharm Techs, for example) required, where applicable.
  • Current certification in Good Clinical Practice (GCP) and/or willingness to complete GCP training
  • Experience with IWRS/IRT systems, inventory control
  • Strong organizational and documentation skills with high attention to detail
  • Proficient in Microsoft Office and electronic data capture systems
  • Ability to follow protocols, SOPs, and maintain regulatory compliance
  • Strong communication and interpersonal skills
  • Demonstrated ability to manage multiple tasks efficiently and work independently or as part of a team
  • Professionalism, reliability, and commitment to patient safety and data integrity
  • Experience with investigational product handling preferred
  • Familiarity with Phase I-IV clinical trials and regulatory requirements an asset
  • Experience in a clinical research or hospital setting preferred

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Need Assistance?
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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