> Markdown version of [/jobs/ext/225887-data-entry-clinical-research](https://www.wearedevelopers.com/jobs/ext/225887-data-entry-clinical-research). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md).

---

# Data Entry - Clinical Research

- **Company:** CenExel Clinical Research
- **Location:** Anaheim, CA, United States
- **Experience:** Starter
- **Salary:** $41,600.0 - $44,720.0
- **Contract:** Permanent contract
- **Skills:** Coherent Remote File System (CRFS), Electronic Data Capture
- **Published:** May 29, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=4816d3dd95dab018

## About the Role

Do you have experience in Medical terminology?, Do you have a High school diploma or GED?, * Minimum High School graduate or equivalent.

 * One year of data entry or related preferred.
 * Must have excellent computer skills and medical/research terminology.
 * Must be self-directed and able to work with minimal supervision.
 * Motivated to work consistently in a fast paced and rapidly changing environment.
 * Able to manage multiple projects and responsibilities.

Working Conditions

 * Indoor, Office environment.
 * Essential physical requirements include sitting, typing, standing, and walking.
 * Lightly active position, occasional lifting of up to 20 pounds.
 * Reporting to work, as scheduled, is essential.

## Description

Transcribes clinical research data correctly from source documents to electronic data capture following ALCOA-C principles., * Comply with current protocols, SOPs, GCPs, IRB, FDA guidelines, and site training program.

 * Ensure timely data entry through department and study tracking, etc.
 * Maintain healthy professional relationships with Clinical Operations, Quality, Regulatory, CROs, Sponsors, etc., as well key clinical trial personnel.
 * Transcribe data correctly and efficiently from source documents to electronic data capture.
 * Assist in preparing for internal and external data audits along with the clinical operations/ quality/ and regulatory teams.
 * Complete training and obtains applicable certificates and access to CRFs/EDC.
 * Verification of source documents (e.g., "buddy check").
 * Assist CRCs in entering data from paper source documents to eCRFs correctly, accurately and on a timely manner for multiple clinical trials.
 * Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.


## Related Videos

- [Training Bots on Deliveroo Data, Alexa Can Swear and Mushroom Electronics - Julia Kordick](https://www.wearedevelopers.com/videos/1839-training-bots-on-deliveroo-data-alexa-can-swear-and-mushroom-electronics-julia-kordick)

## Related Articles

- [Fully Remote Software Engineer Jobs](https://www.wearedevelopers.com/magazine/447-fully-remote-software-engineer-jobs)
- [Data Analyst Salary in the UK](https://www.wearedevelopers.com/magazine/278-data-analyst-salary-in-the-uk)
- [Where to Find Entry-Level Software Engineering Jobs](https://www.wearedevelopers.com/magazine/397-where-to-find-entry-level-software-engineering-jobs)
- [React Developer Salary [2023]](https://www.wearedevelopers.com/magazine/198-react-developer-salary-2023)
- [Starter Kit For Job Applications For Developers](https://www.wearedevelopers.com/magazine/7-starter-kit-for-job-applications-for-developers)
- [Best Paying Remote Jobs](https://www.wearedevelopers.com/magazine/255-best-paying-remote-jobs)