Remote Clinical Data Coordinator

Care Access

Oregon

Hybrid

USD 36,000 - 50,000

Full time

9 days ago

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Benefits offered by this job

PTO and holidays
Employer-paid health, dental, and vis
HSA and employer contributions
Disability insurance
401(k) with company match

Job summary

Care Access is hiring a Data Coordinator to join a remote, US-based team. You will ensure data quality across clinical trials, perform source data reviews, and support timely data entry into EDC/CRF systems.

This role emphasizes accuracy, documentation, and cross-functional collaboration. You will reconcile data with source records, manage queries, and contribute to study coordination and QC activities across the site network.

Qualifications

  • Minimum high school diploma or GED required; associate or bachelor's preferred.
  • 2+ years experience in clinical research, clinical trial support, or data coordination.
  • Familiarity with EDC systems, case report forms, and data management practices.
  • Ability to work remotely with strong communication and organization.

Responsibilities

  • Perform site-level quality control of source data and resolve discrepancies with staff.
  • Reconcile study data against supporting documentation and track resolution.
  • Enter study data into sponsor EDC/CRF systems accurately and on time.
  • Manage EDC queries, route and respond, ensuring timely closure.
  • Coordinate study activities with study teams and site personnel.
  • Support data quality, reporting, and process improvement tasks.

Skills

Attention to detail
Time management
Communication
Independent worker
Organization
Remote collaboration

Education

High school diploma or GED
Associate or Bachelor's in life sciences or related field

Tools

EDC/CRF systems
Spreadsheets
Project trackers

Job description

Care Access is hiring a Data Coordinator to join a remote, US-based team. You will ensure data quality across clinical trials, perform source data reviews, and support timely data entry into EDC/CRF systems.

This role emphasizes accuracy, documentation, and cross-functional collaboration. You will reconcile data with source records, manage queries, and contribute to study coordination and QC activities across the site network.

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