Celerion7mo ago

From $21/yr

Clinical Data Specialist

United States·LincolnFull-Timemid

OtherHealthcareClinical Data Specialist

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Quick Summary

Overview

The Clinical Data Specialist is responsible for the review of all source data and ensure all applicable data is entered into its respective database and/or Case Report Form (CRF).

Technical Tools

gcpms-office

The Clinical Data Specialist is responsible for the review of all source data and ensure all applicable data is entered into its respective database and/or Case Report Form (CRF). Ensure the completeness, accuracy, and consistency of source data and CRF data entry so that it meets the standard of quality expected for reporting to Sponsors and regulatory bodies. Participate with auxiliary teams involved in study set up, conduct, and data cleaning of clinical trials.

This is an entry level position that pays $21/hour.

Attend study setup meetings to determine QC criteria and timelines for each study

Review study-specific source documents to ensure all forms are accurate prior to study start and that all data collected is in accordance with study-specific Case Report Forms and protocol requirements.

Ensure QC reviews are complete in accordance with study-specific timelines

Review source data on an ongoing basis to ensure the following: Clinical source data is complete according to GCP and FDA guidelines, protocol deviations (if applicable) are documented, and source data is collected in accordance with Sponsor requirements, and Celerion SOPs/PGs.

Ensure data corrections are completed according to GCP guidelines, and Celerion SOPs/PGs.

Complete a Final QC to ensure all source data is accounted for and has been QC reviewed.

Perform accurate data entry and verification for Celerion Standard and Sponsor Provided EDCs.

Archive source documentation including CRFs.

Complete QC/DE dedicated milestones in a timely manner.

Perform standard quality control steps.

High School Diploma or GED (relevant internal Celerion experience in lieu preferred).

1 - 2 years industry experience preferred.

Previous Quality Control/ Data Entry or related experience preferred.

Medical Terminology Training preferred.

Excellent oral and written communication skills.

Ability to organize and manage multiple priorities.

Experience working in an environment with complex processes and defined criteria.

Excellent time management skills required.

Proficient in MS Office applications required.

Excellent attention to detail skills required.

Location & Eligibility

Where is the job

Lincoln, United States

On-site at the office

Who can apply

Listed under

United States

Listing Details

Posted: October 27, 2025
First seen: April 6, 2026
Last seen: May 26, 2026

Posting Health

Days active: 50
Repost count: 0
Trust Level: 41%
Scored at: May 26, 2026

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Celerion

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Celerion is a leading Clinical Research Organization focused on accelerating early phase drug development through innovative strategies and comprehensive research services.

Employees

3k+

Founded

2010

Domain

celerion.com

Jobs

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Salary

From $21

per year