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# Data Coordinator

- **Company:** Start Inc.
- **Location:** Fort Worth, TX, United States
- **Experience:** Experienced
- **Contract:** Permanent contract
- **Skills:** Software Applications, Clinical Data Repository, Computer Literacy, Coherent Remote File System (CRFS), File Systems
- **Published:** July 9, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=99b366842ce268a6

## About the Role

* High School Diploma/GED.

 * 2 years of clinical data entry experience.

 * Knowledge and training in general office administration skills, including computer applications, filing systems., etc.

Preferred Education and Experience:

 * Bachelor's degree.

 * Ability to accurately perform data review and CRF completion in its entirety with minimal direction.

 * Familiarity with medical terminology. CCRP or CCRC credentials is highly desirable.

Physical and Travel Requirements:

 * Travel required up to 10% of the time.

 * Sitting for extended periods of time.

 * Typing and computer use for extended periods of time.

## Description

We are seeking a Data Coordinator. This role will collect, enter/transcribe, and transmit/submit clinical data for assigned investigational drug studies., * Collect, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case report forms (CRFs), including correction and query resolution for assigned investigational drug studies.

 * Receive and request patient records/data from the study team as required to complete CRFs for assigned studies.

 * Review patient data for completeness and accuracy for assigned studies.

 * Coordinate and schedule monitor visits for assigned studies. This includes exit meetings with monitors to review data or queries.

 * Identify lab facilities used for assigned studies and communicate to the Regulatory Affairs staff so that lab certifications can be requested for the study file.

 * Review and utilize protocols as guides for study activities for assigned studies.

 * Assure that data entry remains current for all assigned studies.

 * Attend meetings as required for assigned studies. This includes, but is not limited to, site initiation meetings, monitor exit meetings, close-out visit meetings, and audit preparation meetings.

Other duties may be assigned at any time.


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