Onsite Clinical Data Entry Specialist — EDC & Compliance

ObjectiveGI, Inc.

South Bend (IN)

On-site

USD 36,000 - 54,000

Full time

14 days+

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Job summary

ObjectiveHealth is seeking a Clinical Research Data Entry Specialist to join our onsite team in Indiana. You will enter and verify trial data in EDC systems, support data quality, and help ensure compliance with GCP, HIPAA, and study protocols.

This is ideal for detail-oriented professionals with data entry or administrative background aiming to grow a career in clinical research. You will collaborate with coordinators, investigators, and study staff to resolve data issues, maintain audit

Qualifications

1+ years of data entry, administrative support, medical office, or related experience.
Excellent attention to detail and data accuracy.
Strong written and verbal communication skills.

Responsibilities

Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines.
Review source documents and medical records to ensure complete and accurate transcription of participant data.
Verify data for accuracy, completeness, and consistency prior to submission.
Review, investigate, and resolve EDC data queries generated by sponsors, CROs, or data management teams by comparing source documentation and collaborating with study personnel.
Communicate with Clinical Research Coordinators, investigators, and other study staff to resolve missing, incomplete, or inconsistent data.