PRN Data Coordinator - US - Remote

Worldwide Clinical Trials•San Antonio, TX

4d•$14 - $29•Remote

About The Position

The PRN Data Coordinator is responsible for assuring that the source data captured during a clinical trial has been transcribed into the Case Report Form (CRF) with accuracy and that the data transcription has been completed in accordance with Good Clinical Practice guidelines. The PRN Data Coordinator works under the general supervision and guidance of the Senior Manager, Study Conduct.

Requirements

Excellent written and oral communication skills.
Ability to understand complex written and oral instructions.
Basic computer knowledge and applications required for generation of business correspondence and entry of study data into an electronic Case Report Form.
Strong interpersonal skills.
Excellent attention to detail.
Some knowledge of the clinical research process, including Good Clinical Practices.

Nice To Haves

Experience or class work in the health field.

Responsibilities

Reviews study protocol for studies assigned.
Ensure data from source documents for the trial are accurately reflected on the Case Report Form whether electronic or paper.
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.