> Markdown version of [/jobs/ext/3995520-remote-data-coordinator](https://www.wearedevelopers.com/jobs/ext/3995520-remote-data-coordinator). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md).

---

# Remote Data Coordinator

- **Company:** MEDIX
- **Location:** Newtown, CT, United States
- **Salary:** $58,240.0
- **Contract:** Permanent contract
- **Skills:** Microsoft Word, Microsoft Excel, Clinical Data Repository, Databases, Data Integrity, Electronic Data Capture, Oracle (Applications), Data Management
- **Published:** October 28, 2026
- **Apply:** https://www.thejobnetwork.com/job/8eafcf32-89f9-4e23-8155-1426e724a04e/remote-data-coordinator

## About the Role

* Education & Experience: Bachelor's degree in a related field plus 2 years of relevant experience (or an equivalent combination of education and experience).
 * Technical Skills: Proficiency in Microsoft Excel, Word, and electronic data capture/medical databases.
 * Core Competencies: Strong organization, multitasking ability, self-motivation, and a strict commitment to participant confidentiality and data integrity., * Experience in an oncology or high-volume clinical trials environment.
 * Familiarity with clinical systems (e.g., Medidata Rave, Epic, OnCore, Oracle).
 * Knowledge of GCP guidelines, HIPAA regulations, and IRB standards.

## Description

We are seeking a Clinical Data Coordinator to provide comprehensive data management and administrative support for ongoing clinical trials. This role involves accurate clinical data entry, participant scheduling, and monitoring visit support, requiring independent judgment and strict attention to detail., * Manage end-to-end clinical trial data collection, source verification, and entry into sponsor databases.

 * Coordinate participant appointments and follow-ups across all study phases, from recruitment through post-treatment.
 * Maintain complete, accurate, and audit-ready participant research records.
 * Support monitoring visits and liaise professionally with study sponsors and team members.