Clinical Trial Medical Quality Control/Data Entry Specialist at Renstar Medical Research

Ocala, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

12 Jul, 26

Salary

0.0

Posted On

13 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Data entry, Quality control, Medical terminology, Clinical trial data management, Good clinical practice (GCP), Attention to detail, Microsoft Office, Data integrity, Regulatory compliance, Time management, Organizational skills, Communication, Problem solving, Source document review, Electronic data capture

Industry

Research Services

Description

Description This Isn’t Just Data Entry — It’s Data That Changes Lives Every new treatment depends on data that has to be right—and on someone making sure it is. That could be you. We’re looking for a sharp, detail-driven QC & Data Specialist who wants their work to be meaningful. and brings a strong working knowledge of medical terminology, medications, and disease states. In this role, you won’t just input information; you’ll safeguard the integrity of clinical trial data that directly impacts patient safety, regulatory decisions, and the future of medicine. If you take pride in precision, catch what others miss, and want to be part of research that truly matters, this is your opportunity. What You’ll Do (and Why It Matters) Turn Information into Impact Review source documents and transcribe data with precision into electronic data capture systems Resolve data queries within applicable timelines. Keep critical study records organized, complete, and inspection-ready Champion Data Quality Perform QC reviews to catch discrepancies before they become risks. Identify missing, inconsistent, or incorrect data and follow through on the resolution of discrepancies Help uphold the standards that regulators, sponsors, and patients rely on Protect the Integrity of Research Support compliance with Good Clinical Practice (GCP) and study protocols Maintain confidentiality of patient information and sensitive data. Assist with audit readiness Play a key role in ensuring data is accurate, complete, and audit-ready Collaborate with Purpose Engage and communicate with clinic teams, sponsors, and other pharmaceutical professionals in a collaborative and courteous manner. Work with monitors during on-site visits, supporting source review, data clarification, and query resolution. Be a trusted team member in delivering high-quality research outcomes Who You Are Naturally positive, with a steady and solutions-focused mindset Exceptionally detail-oriented—you notice what others overlook. Motivated by meaningful work, not just task completion Organized, reliable, and able to manage multiple priorities A clear communicator who can follow through and solve problems Requirements What You Bring Required: High school diploma or equivalent Knowledge and prior work history involving medical terminology, medical conditions, and an understanding of medications. 1+ years of experience in data entry, quality control, or administrative support Strong attention to detail and accuracy Proficiency in Microsoft Office Excellent organizational and time management skills Why Join Us Be part of research that advances real treatments and therapies See the direct impact of your work on patient safety and outcomes Grow in a fast-paced, purpose-driven clinical research environment Work alongside a team committed to excellence and integrity

Responsibilities

You will transcribe and review clinical trial data to ensure accuracy and integrity while resolving discrepancies. Additionally, you will support audit readiness and maintain compliance with study protocols and Good Clinical Practice.