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Weekend Lab Data Entry Jobs in North Carolina (NOW HIRING)

Overview Join a dynamic healthcare team as a Lab - Phlebotomist, where your skills will directly ... weekends, holidays, and overtime. Keyboard and data entry experience. Looking for a rewarding ...

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Weekend Lab Data Entry information

What is the difference between Weekend Lab Data Entry vs Weekend Medical Data Entry?

AspectWeekend Lab Data EntryWeekend Medical Data Entry
Required CredentialsHigh school diploma, basic computer skillsHigh school diploma, familiarity with medical terminology
Work EnvironmentLaboratories, healthcare facilitiesHospitals, clinics, healthcare offices
Industry UsageLaboratory testing centersMedical practices and healthcare providers
Common Search IntentData entry jobs in labs on weekendsMedical data entry roles on weekends

Weekend Lab Data Entry involves inputting laboratory test results and related data primarily in lab settings, while Weekend Medical Data Entry focuses on entering patient information and medical records in healthcare environments. Both roles require basic computer skills and are often sought for weekend work, but they serve different healthcare sectors.

What are the most commonly searched types of Lab Data Entry jobs in North Carolina? The most popular types of Lab Data Entry jobs in North Carolina are:
What are popular job titles related to Weekend Lab Data Entry jobs in North Carolina? For Weekend Lab Data Entry jobs in North Carolina, the most frequently searched job titles are:
What job categories do people searching Weekend Lab Data Entry jobs in North Carolina look for? The top searched job categories for Weekend Lab Data Entry jobs in North Carolina are:
What cities in North Carolina are hiring for Weekend Lab Data Entry jobs? Cities in North Carolina with the most Weekend Lab Data Entry job openings:

Data Entry Coordinator

Joint and Muscle Medical Care

Charlotte, NC • On-site

$17/hr

Full-time

Posted yesterday

New


Job description

Clinical Research Data Entry Coordinator — Job Description
Summary

The Clinical Research Data Entry Coordinator supports clinical trials by ensuring timely, accurate, and compliant entry of study data into electronic data capture (EDC) systems. This role works closely with study coordinators, investigators, and monitors to maintain high‑quality documentation and uphold regulatory standards across all assigned studies.
Key Responsibilities
  • Data Entry & Verification — Enter source data into EDC systems (e.g., Medidata Rave, REDCap, Inform) with high accuracy; perform ongoing data cleaning and query resolution.
  • Source Documentation Review — Compare source documents against EDC entries to ensure consistency and completeness.
  • Query Management — Respond to data queries from sponsors/CROs within required timelines; collaborate with clinical staff to obtain missing information.
  • Regulatory Compliance — Maintain adherence to GCP, ICH guidelines, and site SOPs; ensure audit‑ready documentation.
  • Study Support — Assist coordinators with visit documentation, data reconciliation, and tracking of study milestones.
  • Data Quality Assurance — Conduct periodic data reviews, identify trends or recurring issues, and escalate concerns to study leadership.
  • Communication & Collaboration — Work with investigators, coordinators, and monitors to ensure smooth data flow and timely completion of study deliverables.
  • Administrative Tracking — Maintain logs for data entry progress, outstanding queries, and visit completion status.
Required Qualifications
  • Education — Associate’s or Bachelor’s degree in a health‑related field (biology, public health, nursing, etc.).
  • Technical Skills — Experience with EDC platforms; proficiency in Microsoft Excel and basic data management.
  • Attention to Detail — Demonstrated accuracy in data‑heavy environments.
  • Clinical Research Knowledge — Understanding of GCP, ICH, and basic clinical trial workflow.
  • Communication Skills — Ability to collaborate with cross‑functional teams and communicate data needs clearly.
Preferred Qualifications
  • Prior Clinical Research Experience — Experience in a research site, CRO, or academic research setting.
  • Familiarity with Medical Terminology — Ability to interpret clinical notes and lab reports.
  • Experience with Query Resolution — Proven ability to manage sponsor/CRO queries efficiently.
Core Competencies
  • Accuracy & Thoroughness

  • Time Management

  • Confidentiality

  • Problem Solving

  • Process Improvement

Optional Add‑Ons (Depending on Your Use Case)
If you want, I can also generate:
  • A resume bullet list

  • A job posting version

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  • A career progression map

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