Data Coordinator

Worldwide Clinical Trials

Data Coordinator ensuring data is accurately transcribed into Case Report Forms at Worldwide Clinical Trials. Responsible for data management and adherence to Good Clinical Practice guidelines.

Posted 7/8/2026part-timeRemote • Texas • 🇺🇸 United StatesMid-LevelSenior💰 $14 - $29 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in reviewing study protocols and ensuring accurate data representation in Case Report Forms. Proficient in managing source documents and conducting reconciliation of study records within a phase I clinical environment.

Highest-signal resume keywords

Bachelor’s Degree In Life SciencesExperience In Phase I Clinical EnvironmentData ManagementSource Document ReviewProblem Identification

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data Accuracy VerificationStudy Protocol ReviewCase Report Form ManagementRecord Reconciliation

Soft Skills

Problem-SolvingCommunication

Industry Keywords

Clinical TrialsHealth FieldLife Sciences

About the role

Key responsibilities & impact

Reviews study protocol for studies assigned
Ensure data from source documents for the trial are accurately reflected on the Case Report Form
Keep track of source documents being filed into subject folders
Assistance with reconciliation of study records for archive
Identifies problems or potential problems and reports them to his/her supervisor
Responsible for requesting, scheduling and attending any training required for this position

Requirements

What you’ll need

Bachelor’s degree or associate Degree (preferably in the field of Life Sciences or Health)
Experience in a phase I clinical environment
Preferred: Experience or class work in the health field

Benefits

Comp & perks

Competitive benefits package depending on location
Health insurance
Retirement plans