Clinical Data Specialist

TL;DR

Clinical Data Specialist: Review source data and ensure accurate entry into databases and CRFs for early clinical research trials with an accent on completeness, accuracy, consistency, and compliance with GCP, FDA, and sponsor requirements. Focus on performing QC reviews, documenting protocol deviations, completing data corrections, and final verifications.

Location: Onsite in Lincoln, NE

Salary: $21/hour

Company

Clinical research organization specializing in early-phase trials and data management.

What you will do

• Attend study setup meetings to define QC criteria and timelines.
• Review source documents for accuracy prior to study start and ongoing basis per protocol, GCP, and SOPs.
• Perform data entry and verification into EDCs, complete corrections, and final QC.
• Archive source documentation and meet all study milestones.
• Ensure data meets quality standards for sponsors and regulators.

Requirements

• High School Diploma or GED (relevant hirify.global experience preferred).
• 1-2 years industry, QC, or data entry experience preferred.
• Medical terminology training preferred.
• Excellent communication, organization, time management, and attention to detail.
• Proficient in MS Office; experience with complex processes.