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RN Clinical Research Coordinator

Job in Asheville, Buncombe County, North Carolina, 28801, USA
Listing for: Niktor LLC
Full Time position
Listed on 2026-06-10
Job specializations:
  • Nursing
Job Description & How to Apply Below
:pointer-events-auto content-visibility:auto supports- content-visibility:auto : contain-intrinsic-size:  scroll-mb- calc(var( scroll-root-safe-area-inset-bottom,0px)+var( thread-response-height scroll-mt- calc(var( header-height)+min(200px,max(70px,20svh " dir="auto" data-turn-="request-WEB:af65416a-0362-4d51-bdec-737-22" data-testid="conversation-turn-2" data-scroll-anchor="false" data-turn="assistant"> RN Clinical Research Coordinator III

Location:

Asheville, NC 28806

Schedule:

Monday Friday 8:00 AM 5:00 PM
Job Type: Permanent Full-Time
Salary Range: $70,000 $ 90,000 Annually

We are seeking an experienced Registered Nurse Clinical Research Coordinator III to support oncology clinical trials in Asheville, North Carolina. This role is responsible for coordinating and managing Phase 1 3 clinical research studies under the supervision of the Principal Investigator while ensuring compliance with FDA, ICH/GCP, and IRB regulations.

Key Responsibilities
  • Coordinate patient care for oncology clinical research protocols
  • Review study protocols and ensure compliance with study requirements
  • Screen and assess patients based on inclusion/exclusion criteria
  • Conduct informed consent discussions and maintain accurate study documentation
  • Monitor, document, and report adverse events and safety concerns
  • Manage investigational products, study medications, and research specimens
  • Maintain regulatory documents and support IRB submissions
  • Ensure data accuracy and integrity in EDC/CTMS systems
  • Support monitoring visits, audits, and CAPA processes
  • Assist with research budgets and billing compliance
Requirements
  • Active Registered Nurse (RN) License
  • ASN or BSN required
  • Minimum 2 years of nursing experience required
  • Oncology experience preferred
  • Clinical research experience strongly preferred
  • Knowledge of FDA, ICH/GCP, and IRB regulations
  • Experience with EMR, EDC, and CTMS systems preferred
  • Strong communication, organizational, and critical thinking skills
  • Valid Driver s License required
Preferred Skills
  • Experience with Phase 1 3 clinical trials
  • Ability to work independently in a fast-paced multi-site environment
  • Strong attention to detail and documentation accuracy
Additional Information
  • Day Shift Full-Time
  • No holiday coverage required
  • State License:
    Upon Acceptance
  • Bilingual not required

If you are interested or know someone who may be a good fit, please apply today.

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