# EDC Data Entry Specialist at UniTriTeam

> Remote · EMEA · Junior · Other · open. Source: https://alderhq.app/jobs/greenhouse%3Aunitriteam%3A4094583009 (read 2026-11-10).

## Facts (observed)

- Company: [UniTriTeam](https://alderhq.app/companies/unitriteam)
- Location text: Bogota, Colombia; Buenos Aires, Argentina; Cairo, Egypt; DF, Mexico; Remote: EMEA
- Where it can be done from (inferred): Remote · EMEA (evidence: "Location: Bogota, Colombia; Buenos Aires, Argentina; Cairo, Egypt; DF, Mexico; Remote: EME")
- Posted: 2026-01-12 (301 days ago)
- First seen by alder: 2026-11-07 · last verified: 2026-11-08
- Reposted: 0 times · edited: 0 times
- Apply on the employer's site: https://job-boards.greenhouse.io/unitriteam/jobs/4094583009
- Skills listed (inferred): GCP

## Pay and sponsorship

- Posted pay: not posted

## Description (the employer's text)

### EDC Data Entry Specialist (Remote – PST/CST/EST Hours)

### Company

UniTriTeam – Supporting Clinical Research Excellence

### About the Role

UniTriTeam is hiring for multiple remote EDC Data Entry Specialist roles to support our clinical research clients across the U.S. These full-time remote positions require availability during standard business hours in Pacific (PST), Central (CST), or Eastern (EST) time zones.

We’re looking for meticulous, detail-oriented professionals with a medical background and a passion for data accuracy. In this role, you'll be responsible for entering and verifying clinical trial data in EDC systems, maintaining the highest standards of data integrity.

### Key Responsibilities

- Accurately enter clinical trial data into Electronic Data Capture (EDC) systems in compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Perform validation and quality checks to ensure data completeness and accuracy.
- Work collaboratively with clinical research coordinators and site staff to resolve discrepancies.
- Maintain strict confidentiality and security of all clinical trial data.
- Generate data reports and summaries for site and study team review as needed.
- Keep current on all study-related documents and database/system updates.
- Complete all study-required trainings as instructed by the clinical research site team.
- Follow all Standard Operating Procedures (SOPs) and suggest improvements to optimize workflows.
### Required Qualifications

### Education & Experience

- Medical background (degree or relevant professional experience) is required.
- Prior data entry experience in clinical research or healthcare is highly preferred.
### Technical Skills

- Experience with EDC platforms such as Medidata RAVE, REDCap, or similar systems is highly preferred.
- Proficiency with Microsoft Office Suite (Word, Excel, Outlook).
### Core Competencies

- Excellent attention to detail and high degree of accuracy.
- Ability to work under tight deadlines in a regulated environment.
- Effective communication skills and a collaborative spirit.
- Familiarity with clinical trial processes and medical terminology is a plus.
### Why Join Us?

UniTriTeam is a global leader in providing operational, administrative, and technology support to clinical research sites. We take pride in our mission to help advance medicine and make a real impact in healthcare. By joining our team, you’ll benefit from:

- A collaborative and supportive work environment
- Opportunities for professional growth and advancement
- A chance to be part of meaningful research initiatives that change lives

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Data: alder (https://alderhq.app). Cite https://alderhq.app/jobs/greenhouse%3Aunitriteam%3A4094583009 and the date you read it. Observed facts come from the employer's own listing; location reach, level, family and skills are inferences.