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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. About Navitas Healthcare, LLC: It is a certified WBENC and one of the fastest-growing healthcare staffing firms in the US providing Medical, Clinical and Non-Clinical services to numerous hospitals.

YEAR

<p><strong>Job Title:</strong> RN Clinical Research Coordinator III</p><p><strong>Location:</strong> Asheville, NC</p><p><strong>Job Type:</strong> Permanent</p><p><strong>Schedule:</strong> Monday – Friday | 8:00 AM – 5:00 PM</p><h3>Compensation:</h3><ul><li><strong>Salary Range:</strong> $72,000 – $93,000 annually<br/><em>Compensation based on experience and qualifications</em></li></ul><h3>Position Overview:</h3><p>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.</p><h3>Responsibilities:</h3><h4>Protocol Comprehension & Study Coordination:</h4><ul><li>Coordinate patient care activities for clinical trial participants in accordance with GCP guidelines, ICH/FDA regulations, and study protocols</li><li>Conduct protocol feasibility assessments and complete site qualification questionnaires</li><li>Evaluate patient eligibility based on protocol inclusion and exclusion criteria</li><li>Conduct informed consent discussions and ensure regulatory compliance</li><li>Review diagnostic results and maintain required protocol documentation</li><li>Identify and proactively address risks related to protocol non-compliance</li></ul><h4>Adverse Event & Investigational Product Management:</h4><ul><li>Identify, assess, document, and report adverse events (AE), serious adverse events (SAE), and safety concerns</li><li>Dispense investigational medications according to study protocols</li><li>Manage investigational product inventory, storage, accountability, and destruction processes</li><li>Ensure investigational products are stored and documented in compliance with federal regulations and study requirements</li></ul><h4>Regulatory & Data Integrity:</h4><ul><li>Prepare and maintain IRB/IEC documentation throughout the study lifecycle</li><li>Ensure compliance with sponsor reporting requirements and regulatory standards</li><li>Collect, record, and report accurate clinical research data</li><li>Protect patient rights, confidentiality, and study integrity</li><li>Coordinate monitoring visits and maintain communication with sponsors and research teams</li><li>Implement and monitor corrective and preventive action (CAPA) plans</li><li>Escalate protocol deviations and compliance concerns appropriately</li></ul><h4>Financial & Budget Support:</h4><ul><li>Assist with clinical trial budget development and financial tracking</li><li>Support research billing compliance and contract execution processes</li><li>Understand study payment terms, invoicing procedures, and sponsor agreements</li></ul><h3>Qualifications:</h3><h4>Education:</h4><ul><li>High School Diploma required</li><li>Associate Degree in Nursing (ASN) or Bachelor of Science in Nursing (BSN) required</li></ul><h4>Licensure & Certifications:</h4><ul><li>Current Registered Nurse (RN) license required</li><li>Valid driver’s license required</li><li>Must comply with organizational driver safety and motor vehicle policies</li></ul><h4>Experience:</h4><ul><li>Minimum 2–5 years of nursing experience required</li><li>Oncology nursing experience preferred</li><li>Clinical research coordination experience strongly preferred</li></ul><h3>Core Competencies:</h3><h4>Critical Thinking & Organization:</h4><ul><li>Strong analytical, organizational, and problem-solving skills</li><li>Ability to manage multiple priorities independently in a fast-paced environment</li><li>High attention to detail and documentation accuracy</li></ul><h4>Communication & Collaboration:</h4><ul><li>Excellent written and verbal communication skills</li><li>Strong interpersonal and conflict resolution abilities</li><li>Ability to handle confidential and emotionally sensitive information professionally</li></ul><h4>Technical Skills:</h4><ul><li>Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook required</li><li>Experience with Electronic Medical Records (EMR), Electronic Data Capture (EDC) systems, and Clinical Trial Management Systems (CTMS) preferred</li></ul><p>For more details reach at Aditi.sharma@navitashealth.com or Call / Text at 516-587-6677.</p><p>About Navitas Healthcare, LLC: It is a certified WBENC and one of the fastest-growing healthcare staffing firms in the US providing Medical, Clinical and Non-Clinical services to numerous hospitals. We offer the most competitive pay for every position we cater. We understand this is a partnership. You will not be blindsided and your salary will be discussed upfront.</p>

NavitasPartners

RN Clinical Research Coordinator III - RCRC #004

Adverse Events

Analysis Skills

Billing

Budget Management

Budgeting

Clinical Data

Clinical Information Systems

Clinical Medicine

Clinical Nursing

Clinical Research

Clinical Trial

Clinical Trial Management

Communication Skills

Conflict Resolution

Corrective Action

Corrective and Preventative Action (CAPA) Systems

Detail Oriented

Documentation

Driver's License

Electronic Data Capture (EDC)

Electronic Medical Records

FDA Requirements

Federal Compliance Regulations

GCP (Good Clinical Practices)

Healthcare

High School Diploma

Hospital

ICH Regulations

IRB/IEC (Institutional Review Board/Independent Ethics Committee)

Informed Consent

Interpersonal Skills

Inventory Management

Investigational New Drug (IND)

Maintain Compliance

Medications

Microsoft Excel

Microsoft Outlook

Microsoft PowerPoint

Microsoft Word

Multitasking

Nursing

Oncology

Organizational Skills

Patient Care

Patient Confidentiality

Patient Rights

Phase I Clinical Trials

Phase III Clinical Trials

Presentation/Verbal Skills

Problem Solving Skills

Product Management

Registered Nurse (RN)

Regulatory Compliance

Research Protocols

Safety Compliance

Writing Skills

TalentNest

About Navitas Healthcare, LLC certified WBENC and one of the fastest-growing healthcare staffing firms in the US providing Medical, Clinical and Non-Clinical services to numerous hospitals. This role supports Phase I–III interventional clinical trials and ensures full compliance with Good Clinical Practice (GCP), ICH/FDA regulations, and organizational policies.

<h2>Clinical Research Coordinator III (RN) – Direct Hire</h2><h3>Location</h3><p>Asheville, NC 28806</p><hr/><h3>Schedule</h3><p>Full-Time<br/> Monday – Friday<br/> Day Shift: 8:00 AM – 5:00 PM</p><hr/><h3>Compensation</h3><p>$72,000 – $93,000 annually<br/> Additional compensation and benefits may be available based on experience and organizational guidelines.</p><h3>Position Overview</h3><p>The <strong>Clinical Research Coordinator III (RN)</strong> is responsible for coordinating and managing complex clinical research studies under the medical supervision of the Principal Investigator. This role supports Phase I–III interventional clinical trials and ensures full compliance with Good Clinical Practice (GCP), ICH/FDA regulations, and organizational policies.</p><p>The coordinator works independently with a high level of accuracy and professionalism, ensuring patient safety, protocol adherence, and data integrity throughout all stages of clinical research.</p><hr/><h3></h3><h2>Key Responsibilities</h2><h3>Protocol Comprehension & Study Implementation</h3><ul><li>Coordinate care for patients enrolled in clinical research studies in accordance with GCP and FDA guidelines</li><li>Review protocol requirements and independently execute study procedures accurately</li><li>Conduct feasibility assessments and complete site qualification questionnaires</li><li>Assess patient eligibility using inclusion and exclusion criteria</li><li>Facilitate informed consent and ensure regulatory compliance throughout enrollment</li><li>Review diagnostic testing and protocol-required documentation</li><li>Monitor, document, and report adverse events and serious adverse events</li><li>Manage investigational product handling, including accountability, storage, and documentation</li><li>Oversee specimen collection, processing, and proper documentation</li></ul><hr/><h3>Regulatory Compliance & Data Integrity</h3><ul><li>Prepare and maintain IRB/IEC submissions and regulatory binders</li><li>Ensure compliance with safety reporting and protocol deviation processes</li><li>Accurately collect and enter study data in accordance with FDA standards</li><li>Protect patient confidentiality, rights, and study integrity</li><li>Coordinate monitoring visits, audits, and follow-up requests</li><li>Support CAPA (Corrective and Preventive Action) processes</li><li>Escalate compliance or safety concerns to the Principal Investigator and leadership</li></ul><hr/><h3>Research Financial Management</h3><ul><li>Assist with study budget development and financial feasibility reviews</li><li>Support clinical trial billing compliance and documentation</li><li>Track sponsor payments and assist with invoicing processes</li></ul><hr/><h2>Required Qualifications</h2><h3>Education</h3><ul><li>High School Diploma required</li><li>Associate Degree in Nursing (ASN) or Bachelor of Science in Nursing (BSN) required</li></ul><h3>Licensure & Certifications</h3><ul><li>Active Registered Nurse (RN) license required or eligibility to obtain upon hire</li><li>Valid Driver’s License required</li></ul><h3>Experience</h3><ul><li>Minimum 2 years of nursing experience required</li><li>Oncology experience preferred</li><li>Prior clinical research experience preferred</li></ul><h3></h3><p>For more details contact at <p>hdavda@navitashealth.com</p> or Call / Text at<strong> 516-862-1169.</strong></p><p>About <strong>Navitas Healthcare, LLC</strong> certified WBENC and one of the fastest-growing healthcare staffing firms in the US providing Medical, Clinical and Non-Clinical services to numerous hospitals. We offer the most competitive pay for every position we cater. We understand this is a partnership. You will not be blindsided and your salary will be discussed upfront.</p>

Clinical Research Coordinator III (RN) – Direct Hire - Asheville, NC

Clinical Support

Compensation and Benefits

Data Entry

Data Quality

FDA (Food and Drug Administration)

Financial Management

Leadership

Patient Safety

Regulatory Submissions

Sample/Specimen Processing

Specimen Collection

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RN Clinical Research Coordinator III - RCRC #004NavitasPartners

Clinical Research Coordinator III (RN) – Direct Hire - Asheville, NCNavitasPartners

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