Clinical Trials Data Coord

Role overview

This remote, full-time role supports the accuracy, completeness, and regulatory readiness of data generated by oncology clinical trials. The coordinator manages study information across research systems, works with clinical research stakeholders, and helps ensure that trial activities and records remain consistent with approved protocols.

Responsibilities

- Abstract study data and complete case report forms accurately and on schedule. - Review and resolve data queries, documenting decisions and corrections clearly. - Maintain electronic research records and patient-related study information in clinical trial management systems. - Coordinate sponsor monitoring visits and help prepare documentation for review. - Keep trial data organized and audit-ready throughout study execution. - Escalate protocol deviations, operational concerns, and data-quality issues to the appropriate research staff.

Requirements

- Bachelor’s degree, or equivalent relevant experience in place of the degree. - At least two years of experience supporting or conducting oncology clinical trials. - Working knowledge of clinical research processes, institutional review board requirements, and applicable federal, state, and local regulations. - Understanding of Good Clinical Practice, regulatory expectations, research privacy requirements, and relevant government guidance. - Strong written and verbal communication skills, with the ability to share time-sensitive information accurately. - Excellent organization, prioritization, deadline management, and attention to detail.

Benefits and work setup

- Full-time remote position.