Clinical Data Coordinator - 260070

We are seeking an organized, detail-oriented, and adaptable part-time Clinical Data Coordinator to support electronic data capture (EDC), data entry, query management, and source document verification. In this specialized data management role, you will play a key part in maintaining accurate clinical study databases, resolving data discrepancies, and ensuring timely data entry to support smooth day-to-day trial operations. It is a temporary project-based support contract role.

Responsibilities

• Data Entry & Management: Perform timely and accurate clinical trial data entry from source documents into Electronic Data Capture (EDC) systems in compliance with study protocols and GCP guidelines.
• Query Resolution & Quality Control: Review incoming data for completeness, identify discrepancies, and collaborate with clinical research staff and sponsors to resolve data queries efficiently.
• Source Document Tracking & Administration: Track, organize, and manage source documentation, ensuring all required trial data and medical records are properly reconciled and audit-ready.

Required Qualifications

• Proven experience with clinical data entry across one or more Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle InForm, REDCap).
• Demonstrated experience working on sponsor-funded clinical trials.
• Strong organizational skills with high attention to detail in source document verification and discrepancy management.
• Excellent written and verbal communication skills for cross-functional collaboration and sponsor query resolution.
• Worked in oncology trials in the past

Schedule & Logistics

• Role Type: Temporary project-based contract, roughly 5 months
• Hours: Part-time, 16 hours per week (Day shift between 8:00 AM – 5:00 PM). No evenings or weekends required.
• Schedule: Preferred schedule can be two chosen days between M-F and should stay the same week by week.