Remote Oncology Trials Data Coordinator

City of Hope

United States

Remote

USD 65,000 - 90,000

Full time

14 days+

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Benefits offered by this job

Fully remote

Job summary

City of Hope is seeking a remote Data Coordinator to ensure the accuracy, completeness, and regulatory readiness of data generated by oncology clinical trials. The coordinator manages study information across research systems, collaborates with trial stakeholders, and helps ensure that trial activities and records stay aligned with approved protocols.

The role involves abstracting data, resolving data queries, maintaining electronic records in trial management systems, and coordinating sponsor

Qualifications

  • Bachelor’s degree or equivalent experience.
  • At least two years of experience in oncology clinical trials.
  • Working knowledge of clinical research processes, IRB requirements, and applicable regulations.
  • Understanding of Good Clinical Practice and privacy regulations.
  • Strong written and verbal communication; ability to share time-sensitive information accurately.
  • Excellent organization, prioritization, deadline management, and attention to detail.

Responsibilities

  • Abstract study data and complete case report forms on schedule.
  • Review and resolve data queries with clear documentation.
  • Maintain electronic records and trial information in CTRMs.
  • Coordinate sponsor monitoring visits and prepare documentation.
  • Keep trial data organized and audit-ready throughout the study.
  • Escalate deviations and data-quality issues to the research staff.

Skills

Communication
Attention to detail
Time management

Education

Bachelor’s degree or equivalent experience

Job description

City of Hope is seeking a remote Data Coordinator to ensure the accuracy, completeness, and regulatory readiness of data generated by oncology clinical trials. The coordinator manages study information across research systems, collaborates with trial stakeholders, and helps ensure that trial activities and records stay aligned with approved protocols.

The role involves abstracting data, resolving data queries, maintaining electronic records in trial management systems, and coordinating sponsor

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