Registered Nurse - Research
iDeal Hire · idealhire.com
AshevilleMid level2–5 yrs
The job in short
Clinical research nurse.
GCPExcelNursingClinicalCompliance
Details
- Found
- 11 d ago · posted 2026-09-18
- Location as listed
- Asheville, NC
- Role
- Lab / Clinical Research
- Source
- The company’s own careers site
Full description
Job Title
• Clinical Research Coordinator III (RN)
Location
• Asheville, NC
Schedule / Job Type
• Full-time, Day shifts, 1 shift per week
Key Responsibilities
• Perform study-related duties under the supervision of the Principal Investigator for complex clinical research protocols (phases 1-3 interventional trials) in accordance with GCP, ICH, and FDA guidelines.
• Screen and assess study candidates for eligibility based on inclusion/exclusion criteria, and evaluate diagnostic test results.
• Conduct informed consent discussions and review documentation with participants, ensuring compliance with regulatory requirements.
• Manage and dispense investigational medications responsibly, maintaining accurate inventory and records per sponsor guidelines and CFR standards.
• Document and report adverse events, ensuring appropriate follow-up, causal assessment, and sponsor/IRB reporting.
• Support regulatory compliance by maintaining IRB/IEC documents, certifications, and site credentials, and manage data integrity throughout the study lifecycle.
Required Qualifications
• Registered Nurse license (RN) with valid state licensure in North Carolina.
• High school diploma or equivalent; ASN or BSN required.
• 2-5 years of nursing experience, with preference for oncology background.
• Valid driver’s license for travel to satellite offices and offsite meetings.
Preferred Experience / Skills
• Prior experience with electronic medical records (EMR), clinical trial data entry systems (EDC), or Clinical Trial Management Systems (CTMS).
• Demonstrated critical thinking, analytical skills, and attention to detail.
• Strong interpersonal, communication, and organizational skills, with ability to handle sensitive and confidential information.
• Proficiency in MS Office Suite (Word, Excel, PowerPoint, Outlook).
Why Join Us
• Opportunity to contribute to impactful clinical research in a dynamic, multidisciplinary team environment.
• Supportive organization committed to professional growth, compliance, and excellence in patient care.
Warnings
• Do not include personal names or contact details.
• Do not add pay rates, salaries, or specific company or facility names.
• Only include city and state for location; no full addresses or contact info.
• Maintain a professional and compliant tone suitable for public job postings.
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