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