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RN Clinical Research Coordinator III - RCRC #004

NavitasPartners
locationHendersonville, NC, USA
PublishedPublished: 6/14/2022
Healthcare
Full Time

Job Description

Job Description

Job Title: RN Clinical Research Coordinator III

Location: Asheville, NC

Job Type: Permanent

Schedule: Monday – Friday | 8:00 AM – 5:00 PM

Compensation:

  • Salary Range: $72,000 – $93,000 annually
    Compensation based on experience and qualifications

Position Overview:

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.

Responsibilities:Protocol Comprehension & Study Coordination:

  • 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

Adverse Event & Investigational Product Management:

  • 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

Regulatory & Data Integrity:

  • 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

Financial & Budget Support:

  • 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

Qualifications:Education:

  • High School Diploma required
  • Associate Degree in Nursing (ASN) or Bachelor of Science in Nursing (BSN) required

Licensure & Certifications:

  • Current Registered Nurse (RN) license required
  • Valid driver’s license required
  • Must comply with organizational driver safety and motor vehicle policies

Experience:

  • Minimum 2–5 years of nursing experience required
  • Oncology nursing experience preferred
  • Clinical research coordination experience strongly preferred

Core Competencies:Critical Thinking & Organization:

  • 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

Communication & Collaboration:

  • Excellent written and verbal communication skills
  • Strong interpersonal and conflict resolution abilities
  • Ability to handle confidential and emotionally sensitive information professionally

Technical Skills:

  • Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook required
  • Experience with Electronic Medical Records (EMR), Electronic Data Capture (EDC) systems, and Clinical Trial Management Systems (CTMS) preferred

For more details reach at Aditi.sharma@navitashealth.com or Call / Text at 516-587-6677.

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.

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