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# Study Report Data Specialist - Part Time / Daytona Beach, FL (On-Site)

- **Company:** Fortrea Inc.
- **Location:** Daytona Beach, FL, United States
- **Experience:** Starter
- **Contract:** Permanent contract
- **Skills:** Software Applications, Clinical Data Repository, Technical Data Management Systems
- **Published:** August 4, 2026
- **Apply:** https://jobs.localjobnetwork.com/apply/add/87964620/1

## About the Role

* High School Diploma or equivalent
 * 1-2 years experience specific to CRF data and case reporting, industry experience, sponsor experience
 * Clinical Research experience is preferred

The important thing for us is you are comfortable working in an environment that is:

 * Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
 * Changing priorities constantly asking you to prioritize and adapt on the spot.
 * Teamwork and people skills are essential for the study to run smoothly.
 * Technology based. We collect our data directly into an electronic environment., * Ability to work in an upright and /or stationary position for 6-8 hours per day.
 * Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
 * Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
 * Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
 * Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
 * Regular and consistent attendance.
 * Varied hours may be required.

## Description

You will utilize your skills, knowledge, and clinical judgement for all aspects of data capture, review and quality for Phase I studies. The Clinical Data Monitor I is someone who ensures that all data and information is produced on time, in accordance with defined quality standards and meets the requirements of the business and our customers., * Transcribe study data into case report form

 * Enter data into the computer using the currently defined data management software.
 * Work in conjunction with study coordinators, quality, and project manager to ensure that case report form completion timelines are met.
 * Work with sponsors during monitoring visits to ensure all data questions and clarifications are answered.
 * Timely follow-up and resolution to all sponsor generated data queries
 * Constantly look for ways to improve the efficiency and quality of unit work processes.
 * And perform other related duties as assigned.


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