Clinical Research Coordinator III (RN) - Asheville, NC - Direct Hire/ Full Time

NavitasPartners

Asheville, NCFull-timePosted May 16, 2026

6,000–7,750 a month

Behavioral Health Market Context

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Benefits

Pay Rate: $72,000 – $93,000 annuallyYou will not be blindsided and your salary will be discussed upfront

Job Description

Job Title: Clinical Research Coordinator III (RN) – Direct Hire

Location: Asheville, NC

Type: Direct Hire / Full-Time

Pay Rate: $72,000 – $93,000 annually

Shift: Day Shift | Hours: 8:00 AM – 5:00 PM | Schedule: Monday – Friday

Position Overview:

Navitas Healthcare, LLC is seeking Clinical Research Coordinator III (RN) for an exciting Travel or Local job in Asheville, NC.
Key Responsibilities
• Coordinate care for patients enrolled in clinical research studies in accordance with GCP and FDA guidelines
• Review protocol requirements and execute study procedures accurately
• Conduct feasibility assessments and complete site qualification questionnaires
• Assess patient eligibility using inclusion and exclusion criteria
• Facilitate informed consent and ensure regulatory compliance throughout enrollment
• Review diagnostic testing and protocol-required documentation
• Monitor, document, and report adverse events and serious adverse events
• Manage investigational product handling, including accountability, storage, and documentation
• Oversee specimen collection, processing, and proper documentation
• Prepare and maintain IRB/IEC submissions and regulatory binders
• Ensure compliance with safety reporting and protocol deviation processes
• Accurately collect and enter study data in accordance with FDA standards
• Protect patient confidentiality, rights, and study integrity
• Coordinate monitoring visits, audits, and follow-up requests
• Support CAPA (Corrective and Preventive Action) processes
• Escalate compliance or safety concerns to the Principal Investigator and leadership
• Assist with study budget development, financial feasibility reviews, and billing compliance
• Track sponsor payments and assist with invoicing processes

Required Qualifications
• High School Diploma required; Associate Degree in Nursing (ASN) or Bachelor of Science in Nursing (BSN) required
• Active Registered Nurse (RN) license required or eligibility to obtain upon hire
• Valid Driver’s License required
• Minimum 2 years of nursing experience required
• Oncology experience preferred
• Prior clinical research experience required

For more details contact [email protected] Call / Text at 516-862-1169.
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. 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.

Qualifications

  • High School Diploma required; Associate Degree in Nursing (ASN) or Bachelor of Science in Nursing (BSN) required
  • Active Registered Nurse (RN) license required or eligibility to obtain upon hire
  • Valid Driver’s License required
  • Minimum 2 years of nursing experience required
  • Prior clinical research experience required

Responsibilities

  • Shift: Day Shift | Hours: 8:00 AM – 5:00 PM | Schedule: Monday – Friday
  • Coordinate care for patients enrolled in clinical research studies in accordance with GCP and FDA guidelines
  • Review protocol requirements and execute study procedures accurately
  • Conduct feasibility assessments and complete site qualification questionnaires
  • Assess patient eligibility using inclusion and exclusion criteria
  • Facilitate informed consent and ensure regulatory compliance throughout enrollment
  • Review diagnostic testing and protocol-required documentation
  • Monitor, document, and report adverse events and serious adverse events
  • Manage investigational product handling, including accountability, storage, and documentation
  • Oversee specimen collection, processing, and proper documentation
  • Prepare and maintain IRB/IEC submissions and regulatory binders
  • Ensure compliance with safety reporting and protocol deviation processes
  • Accurately collect and enter study data in accordance with FDA standards
  • Protect patient confidentiality, rights, and study integrity
  • Coordinate monitoring visits, audits, and follow-up requests
  • Support CAPA (Corrective and Preventive Action) processes
  • Escalate compliance or safety concerns to the Principal Investigator and leadership
  • Assist with study budget development, financial feasibility reviews, and billing compliance
  • Track sponsor payments and assist with invoicing processes


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