Data Entry Specialist

Monroe+Biomedical+Research

Posted 3 months ago

Full Time

Louisville, Kentucky

In Person

Smart Summary

Responsibilities

The role involves accurately entering clinical trial data into study systems and resolving data discrepancies. Additionally, the specialist manages the front desk, greeting patients and scheduling appointments.

Qualifications

You have a high school diploma or equivalent and previous data entry experience, ideally in a clinical or healthcare setting. You are proficient in Microsoft Office Suite, possess strong typing skills with a high degree of accuracy, and have excellent organizational and communication abilities.

Must Have Skills for ATS

Data Entry

Clinical Research

EDC

CRIO

Microsoft Office Suite

Excel

Word

Outlook

Job Description

Data Entry Specialist    |📍 Louisville, KY

Monroe Biomedical Research is seeking a detail-oriented and proactive Data Entry Specialist to support our growing clinical research operations in Monroe, NC. As one of the nation’s leading clinical research centers, we are dedicated to advancing treatments for conditions such as Asthma, COPD, Heart Failure, and more. As we continue to expand, we are looking for a motivated individual who is passionate about accuracy, organization, and contributing to meaningful healthcare advancements.

Position Overview

The ideal candidate is highly organized, accurate, and capable of identifying and resolving discrepancies in real time. This individual thrives in a fast-paced environment, takes initiative, and works independently while supporting the overall success of our clinical studies.

Strong attention to detail, critical thinking skills, and a proactive mindset are essential for success in this role.

Key Responsibilities

  • Enter clinical trial data into study-related systems accurately and efficiently
  • Review and resolve data discrepancies to ensure accuracy and timeliness
  • Take ownership of assigned tasks while proactively supporting data integrity initiatives
  • Collaborate with team members to improve clinical operations and workflow efficiency
  • Front desk management.
  • Greet and assist patients, study participants, and visitors professionally
  • Answer and direct phone calls, schedule appointments, and follow up with participants
  • Maintain patient and visitor logs to support an efficient check-in process
  • Keep reception and waiting areas clean, organized, and welcoming

Education

  • High school diploma or equivalent required
  • Associate degree or higher preferred

Experience

  • Previous data entry experience required, preferably in a clinical or healthcare setting
  • Familiarity with clinical research terminology preferred
  • Experience with EDC, CRIO, or similar systems is a plus

Skills

  • Proficiency in Microsoft Office Suite (Excel, Word, Outlook)
  • Strong typing speed and attention to accuracy
  • Excellent organizational and communication skills
  • Ability to multitask and work independently

Benefits

  • Competitive salary
  • 100% company-paid health insurance, including dental coverage
  • Matching 401(k)
  • Convenient office location with easy highway access

Why Join Monroe Biomedical Research?

Join a dynamic and innovative team that is helping shape the future of healthcare through clinical research. Your work will directly contribute to advancing treatments and improving patient outcomes.

Apply today and help us advance science together.

Monroe+Biomedical+Research

Monroe Biomedical Research (MBR) is a multi-specialty clinical research organization operating fully owned research sites. MBR excels in Phase 1-4 cardiometabolic, endocrinology, and respiratory clinical trials, as well as general medicine studies for drugs, medical devices, and diagnostics. Sponsors and CROs partner with MBR for: • Therapeutic excellence: Distinguished investigators and clinical staff with deep experience in specific disease areas and reaching specialty populations. • Reliable execution: Centrally managed multi-site operations to accelerate timelines from startup through closeout, especially for high-volume trials. • Phase 1 capabilities: Specialized facilities for complex early-phase work. • Recruitment and retention expertise: Expert-led programs designed to consistently outperform industry benchmarks. By conducting research with both scientific rigor and genuine respect for the people who make it possible, MBR provides better experiences for everyone involved — from participants to partners. Whether you are a Sponsor evaluating new site partnerships, a CRO building a select network of high-performing sites, or a professional looking to do meaningful work in clinical research, connect with MBR. Learn more at MonroeResearch.com
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