EDC Data Entry Specialist

UniTriTeam

United States

À distance

USD 45 000 - 70 000

Plein temps

14 jours+

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Résumé du poste

UniTriTeam is hiring for multiple remote EDC Data Entry Specialist roles to support our clinical research clients across the United States. These full-time remote positions require availability during Pacific (PST), Central (CST), or Eastern (EST) time zones.

Ideal candidates have a medical background and meticulous attention to data accuracy, with experience entering and verifying data in EDC systems. Join our team to contribute to high-quality clinical data management.

Qualifications

  • Medical background or relevant experience is required.
  • Prior data entry experience in clinical research or healthcare is preferred.
  • Familiarity with EDC platforms and MS Office is expected.

Responsabilités

  • Enter clinical trial data into EDC systems following study protocols.
  • Perform validation checks to ensure data completeness and accuracy.
  • Collaborate with coordinators to resolve data discrepancies.
  • Maintain confidentiality and comply with SOPs.
  • Generate data reports for site and study teams as needed.
  • Stay updated on study documents and system updates.
  • Complete required trainings as instructed by the site team.
  • Suggest workflow improvements to optimize processes.

Connaissances

Attention to detail
Data entry
Communication skills
Team collaboration

Formation

Medical background/experience

Outils

Medidata RAVE
REDCap
Microsoft Word
Microsoft Excel
Outlook

Description du poste

**EDC Data Entry Specialist (Remote –**PST/CST/EST Hours)

Company:

UniTriTeam – Supporting Clinical Research Excellence

About the Role

UniTriTeam is hiring for multiple remote EDC Data Entry Specialist roles to support our clinical research clients across the U.S. These full-time remote positions require availability during standard business hours inPacific (PST), Central (CST), or Eastern (EST)time zones. We’re looking for meticulous, detail-oriented professionals with a medical background and a passion for data accuracy. In this role, you’ll be responsible for entering and verifying clinical trial data in EDC systems, maintaining the highest standards of data integrity.

Key Responsibilities
  • Accurately enter clinical trial data into Electronic Data Capture (EDC) systems in compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
  • Perform validation and quality checks to ensure data completeness and accuracy.
  • Work collaboratively with clinical research coordinators and site staff to resolve discrepancies.
  • Maintain strict confidentiality and security of all clinical trial data.
  • Generate data reports and summaries for site and study team review as needed.
  • Keep current on all study-related documents and database/system updates.
  • Complete all study-required trainings as instructed by the clinical research site team.
  • Follow all Standard Operating Procedures (SOPs) and suggest improvements to optimize workflows.
Required Qualifications
  • Education & Experience

    • Medical background (degree or relevant professional experience) is required.
    • Prior data entry experience in clinical research or healthcare is highly preferred.
  • Technical Skills

    • Experience with EDC platforms such as Medidata RAVE, REDCap, or similar systems is highly preferred.
    • Proficiency with Microsoft Office Suite (Word, Excel, Outlook).
  • Core Competencies

    • Excellent attention to detail and high degree of accuracy.
    • Ability to work under tight deadlines in a regulated environment.
    • Effective communication skills and a collaborative spirit.
    • Familiarity with clinical trial processes and medical terminology is a plus.
Why Join Us?

UniTriTeam is a global leader in providing operational, administrative, and technology support to clinical research sites. We take pride in our mission to help advance medicine and make a real impact in healthcare. By joining our team, you’ll benefit from:

  • A collaborative and supportive work environment
  • Opportunities for professional growth and advancement
  • A chance to be part of meaningful research initiatives that change lives
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