Clinical Trial Nurse – Gilbert, Arizona (Part-Time, Office-Based)
Location: Gilbert, Arizona
Employment Type: Part-Time (8 hours/month, Onsite Support)
Job ID: R1510046
Apply Now
Job Overview
We are seeking an experienced Clinical Trial Nurse to provide essential onsite support for clinical research studies in Gilbert, AZ. The ideal candidate will coordinate and participate in clinical trials, ensuring all activities comply with study protocols, Good Clinical Practice (GCP), sponsor Standard Operating Procedures (SOPs), and applicable federal, state, and local regulations.
This role is ideal for a nursing professional with a strong background in clinical research, patient management, and regulatory compliance who is looking for flexible, part-time engagement in a high-performing research environment.
Key Responsibilities
Provide clinical research support to investigators, assisting with the preparation and execution of assigned studies.
Review study protocols, source documents, and electronic data capture systems to ensure accuracy and compliance.
Collect, submit, and maintain regulatory and ethics documentation in accordance with FDA and other governing bodies.
Recruit, screen, and orient patients for clinical trials, maintaining accurate screening and enrollment logs.
Conduct study visits, perform delegated procedures, and maintain source documentation per GCP/ICH standards.
Manage laboratory testing, specimen collection, and logistical coordination for clinical samples.
Monitor participant safety, report adverse events, and address study-related inquiries proactively.
Conduct complex clinical research procedures, including ECGs, spirometry, vital signs, cardiac telemetry, dose verifications, and questionnaire administration.
Provide guidance and supervision to site staff, ensuring adherence to study protocols, SOPs, and best nursing practices.
Support investigator training and onboarding of new site staff on study-specific procedures and regulatory requirements.
Participate in study audits, monitoring visits, and regulatory inspections to maintain compliance and data integrity.
Assist in site unit budget management, process improvement, and development of research facilities and services.
Experience & Qualifications
Current RN license with clinical experience in a hospital, research, or healthcare setting.
Minimum 2 years of experience in clinical research, clinical trials, or related nursing roles required.
Solid knowledge of GCP, ICH guidelines, FDA regulations, and clinical research SOPs.
Strong patient management, clinical assessment, and procedural skills.
Experience in supervising and mentoring junior staff or research coordinators is preferred.
Excellent organizational, communication, and problem-solving abilities.
Additional Information
Part-time, office-based role requiring onsite presence in Gilbert, AZ.
Pay range: $50.00–$60.00 per hour, depending on experience and qualifications.
Opportunity to work in a collaborative environment with exposure to advanced clinical research studies.
About the Employer
IQVIA is a leading global provider of clinical research services, healthcare intelligence, and commercial insights to the life sciences industry. We connect people, technology, and data to advance medical innovation and improve patient outcomes worldwide.
IQVIA is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Apply Now to join a global leader in clinical research and contribute to advancing healthcare innovation.
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