Celerion6d ago

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USD 21.5–21.5/yr

Clinical Data Specialist

United States·TempeFull-Timemid

OtherClinical Data Specialist

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Quick Summary

Requirements Summary

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,

Technical Tools

OtherClinical Data Specialist

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

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.

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

Celerion Values: Integrity Trust Teamwork Respect

Are you ready to join our team?

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

Location & Eligibility

Where is the job

Tempe, United States

On-site at the office

Who can apply

Listing Details

Posted: May 21, 2026
First seen: May 26, 2026
Last seen: May 27, 2026

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Days active: 0
Repost count: 1
Trust Level: 49%
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

USD 21.5–21.5

per year