Clinical Research Data Entry Specialist
On-siteSouth Bend, Indiana, United States
Job Summary
Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines by reviewing source documents and medical records for complete transcription. Verify data accuracy and consistency prior to submission, then review, investigate, and resolve EDC data queries generated by sponsors, CROs, or data management teams. Communicate with Clinical Research Coordinators and investigators to resolve missing or inconsistent information, correcting discrepancies while maintaining audit trails. Ensure timely completion of entry and query resolution to support study milestones and database lock, while adhering to study protocols, Good Clinical Practice, and regulatory guidelines. Maintain accurate study documentation and confidentiality of participant information.
Required Qualifications
- High school diploma or equivalent
- 1+ years of data entry, administrative support, medical office, or related experience
- Excellent attention to detail and data accuracy
- Strong organizational and time management skills
- Ability to manage multiple priorities and meet deadlines in a fast-paced environment
- Strong written and verbal communication skills
- Legal authorization to work in the US
- E-Verify participant status
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