At UniTriTeam, we believe people make the difference. We support teams in the clinical research space by providing global, remote talent that integrates seamlessly into your workflow. You’ll be part of a company that is mission-driven, people-first, and proud to support breakthroughs in medicine.
EDC Data Entry Specialist
Location
EST (UTC-5) + 2 moreAll locations: EST (UTC-5) | PST (UTC-8) | CST (UTC-6)
Posted
60 days ago
Salary
0
Seniority
Entry Level
Job Description
EDC Data Entry Specialist
UniTriTeam
Role Description 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. Qualifications - Medical background (degree or relevant professional experience) is required. - Prior data entry experience in clinical research or healthcare is highly preferred. - Experience with EDC platforms such as Medidata RAVE, REDCap, or similar systems is highly preferred. - Proficiency with Microsoft Office Suite (Word, Excel, Outlook). - 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. Benefits - 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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