Overview

About the Role:
We are seeking a detail-oriented and highly organized Clinical Research Data Entry & Quality Coordinator to support ongoing clinical trials. This role focuses on data accuracy, documentation, and compliance. (Work is American hours)

Key Responsibilities:
– Perform data entry and ensure accuracy.
– Review clinical data for completeness, consistency, and quality
– Ensure all required study documents are correctly uploaded and filed
– Communicate with sponsors and internal team regarding data queries
– Support overall study compliance

Qualifications:
– Minimum 2 years of office experience
– Strong attention to detail and commitment to accuracy
– Highly organized, reliable, and able to work independently

Ideal Candidate:
A perfectionist-type individual who takes pride in clean, accurate data and high-quality documentation, and is comfortable working in a remote, detail-driven environment.

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