RN Clinical Research Coordinator III - RCRC #004

NavitasPartners•Asheville, NC

1d•Onsite

About The Position

We are seeking an experienced RN Clinical Research Coordinator III to support and manage complex clinical research studies in a fast-paced healthcare environment. This role independently coordinates Phase I–III clinical trials while ensuring compliance with Good Clinical Practice (GCP), ICH/FDA regulations, organizational policies, and study protocols. The ideal candidate will possess strong oncology nursing knowledge, clinical research coordination experience, and excellent organizational and communication skills.

Requirements

High School Diploma required
Associate Degree in Nursing (ASN) or Bachelor of Science in Nursing (BSN) required
Current Registered Nurse (RN) license required
Valid driver’s license required
Must comply with organizational driver safety and motor vehicle policies
Minimum 2–5 years of nursing experience required
Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook required
Strong analytical, organizational, and problem-solving skills
Ability to manage multiple priorities independently in a fast-paced environment
High attention to detail and documentation accuracy
Excellent written and verbal communication skills
Strong interpersonal and conflict resolution abilities
Ability to handle confidential and emotionally sensitive information professionally

Nice To Haves

Oncology nursing experience preferred
Clinical research coordination experience strongly preferred
Experience with Electronic Medical Records (EMR), Electronic Data Capture (EDC) systems, and Clinical Trial Management Systems (CTMS) preferred

Responsibilities

Coordinate patient care activities for clinical trial participants in accordance with GCP guidelines, ICH/FDA regulations, and study protocols
Conduct protocol feasibility assessments and complete site qualification questionnaires
Evaluate patient eligibility based on protocol inclusion and exclusion criteria
Conduct informed consent discussions and ensure regulatory compliance
Review diagnostic results and maintain required protocol documentation
Identify and proactively address risks related to protocol non-compliance
Identify, assess, document, and report adverse events (AE), serious adverse events (SAE), and safety concerns
Dispense investigational medications according to study protocols
Manage investigational product inventory, storage, accountability, and destruction processes
Ensure investigational products are stored and documented in compliance with federal regulations and study requirements
Prepare and maintain IRB/IEC documentation throughout the study lifecycle
Ensure compliance with sponsor reporting requirements and regulatory standards
Collect, record, and report accurate clinical research data
Protect patient rights, confidentiality, and study integrity
Coordinate monitoring visits and maintain communication with sponsors and research teams
Implement and monitor corrective and preventive action (CAPA) plans
Escalate protocol deviations and compliance concerns appropriately
Assist with clinical trial budget development and financial tracking
Support research billing compliance and contract execution processes
Understand study payment terms, invoicing procedures, and sponsor agreements