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

Clinical Research Coordinator III (RN)

• Direct Hire
• Asheville, NC NavitasPartners
• 4.0 Charlotte, NC Job Details Full-time $72,000
• $93,000 a year 21 hours ago Qualifications High school diploma or GED RN experience Driver's License Data collection Full Job Description Clinical Research Coordinator III (RN)
• Direct Hire Location Asheville, NC 28806 Schedule Full-Time Monday

• Friday Day Shift:

  8:00 AM
• 5:00 PM Compensation $72,000
• $93,000 annually Additional compensation and benefits may be available based on experience and organizational guidelines.

Position Overview The Clinical Research Coordinator III (RN) 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. 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. Key Responsibilities Protocol Comprehension & Study Implementation Coordinate care for patients enrolled in clinical research studies in accordance with GCP and FDA guidelines Review protocol requirements and independently 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 Regulatory Compliance & Data Integrity 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 Research Financial Management Assist with study budget development and financial feasibility reviews Support clinical trial billing compliance and documentation Track sponsor payments and assist with invoicing processes Required Qualifications Education High School Diploma required Associate Degree in Nursing (ASN) or Bachelor of Science in Nursing (BSN) required Licensure & Certifications Active Registered Nurse (RN) license required or eligibility to obtain upon hire Valid Driver's License required Experience Minimum 2 years of nursing experience required Oncology experience preferred Prior clinical research experience preferred For more details contact at or 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.