Clinical Trial Nurse – Part-Time
Gilbert, Arizona | Office-Based | Job ID: R1510046**
Position Overview
A leading global clinical research organization is seeking a Part-Time Clinical Trial Nurse to provide onsite support in Gilbert, Arizona for approximately 8 hours per month. This role is responsible for coordinating and executing clinical research activities in accordance with study protocols, contracted work scope, Good Clinical Practice (GCP), sponsor SOPs, and all relevant regulatory requirements.
This opportunity is ideal for experienced nursing professionals looking to contribute to high-quality clinical research in a flexible, part-time capacity.
Key Responsibilities
Clinical Research Coordination
Support investigators in preparing for and conducting assigned clinical studies.
Review study protocols, source documents, CRFs, and electronic data capture systems.
Submit regulatory and ethics documentation required by the FDA and other applicable authorities.
Recruit, screen, and enroll participants while maintaining accurate logs and documentation.
Educate research subjects on study purpose, procedures, visit timelines, and protocol expectations.
Clinical Procedures & Participant Care
Schedule and conduct study visits under the supervision of the Principal Investigator.
Perform delegated clinical procedures including ECGs, spirometry, vital signs, specimen collection, dose verification, and telemetry monitoring.
Manage lab logistics, including specimen preparation and coordination with laboratory partners.
Monitor participant safety, document adverse events, and communicate findings to investigators, study teams, and IRBs.
Data Quality & Compliance
Maintain accurate source documentation aligned with GCP/ICH standards.
Participate in data quality checks, query resolution, and documentation reviews.
Support the site in preparation for monitoring visits, audits, and regulatory inspections.
Ensure adherence to site policies, SOPs, and all clinical research guidelines.
Collaboration, Training & Support
Participate in routine site meetings to ensure study tasks are executed effectively.
Provide support and guidance to junior site staff; ensure nursing practices meet research standards.
Assist with training new investigators or staff on study-specific procedures.
Maintain up-to-date training records and ensure compliance with staff qualification requirements.
Contribute to continuous improvement initiatives, study process reviews, and resource planning.
Skills & Competencies
Strong clinical skill set with proficiency in advanced procedures used in clinical research.
Excellent communication and participant engagement skills.
Thorough understanding of research protocols, documentation standards, and regulatory requirements.
Proven ability to prioritize tasks and maintain accuracy in a fast-paced research environment.
Experience & Qualification Requirements
Active Registered Nurse (RN) license required.
Minimum 1–2 years of clinical nursing experience, preferably with exposure to clinical research.
Familiarity with GCP/ICH guidelines and regulatory processes is preferred.
Experience performing clinical procedures commonly used in research settings is advantageous.
Compensation
Hourly range: $50.00 – $60.00
Compensation is based on experience, education, location, and job-related qualifications.
Additional incentives, bonuses, and health benefits may be available based on role and employment status.
About the Employer
A global leader in clinical research, healthcare intelligence, and advanced data analytics committed to enabling the development and commercialization of innovative medical treatments. The organization promotes an inclusive, equal-opportunity work environment supporting diversity across all protected categories.
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