RN Clinical Research Coordinator
$70k - $90kNiktor LLC
:pointer-events-auto content-visibility:auto supports- content-visibility:auto : contain-intrinsic-size:auto_100lvh R6Vx5W_threadScrollVars 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-id='request-WEB:af65416a-0362-4d51-bdec-737fc2ed9e51-22' 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
- 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
- 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
- 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.
by Jobble
Vacancy posted 1 day ago
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