Clinical Research Administrative Assistant

Posted 19 Days Ago
Be an Early Applicant
Louisville, KY, USA
In-Office
Entry level
Healthtech • Professional Services • Biotech • Pharmaceutical
The Role
Support clinical research operations by entering and reconciling trial data, managing front desk duties, scheduling and greeting participants, maintaining logs, and improving workflow accuracy and efficiency.
Summary Generated by Built In

Clinical Research Administrative Assistant    |📍 Louisville, KY

Monroe Biomedical Research is seeking a detail-oriented and proactive Clinical Research Administrative Assistant 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.

Status: Full Time/ Hourly (non-exempt)

Hours: 8:30 am- 4:00 pm Monday-Friday

Onsite-Louisville

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.

Please apply only once.

Skills Required

  • High school diploma or equivalent
  • Previous data entry experience
  • Proficiency in Microsoft Office (Excel, Word, Outlook)
  • Strong typing speed and accuracy
  • Excellent organizational and communication skills
  • Ability to multitask and work independently
  • Associate degree or higher
  • Familiarity with clinical research terminology
  • Experience with EDC, CRIO, or similar systems
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The Company
58 Employees

What We Do

Monroe Biomedical Research (MBR) is a multi-specialty clinical research organization operating fully owned research sites. The company specializes in conducting Phase 1-4 clinical trials across various therapeutic areas, including cardiometabolic, endocrinology, respiratory, and general medicine research for drugs, medical devices, and diagnostics. MBR partners with sponsors and CROs to deliver high-quality trial execution and a supportive, respectful experience for all research participants.

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