Part Time Research Coordinator Infusion Nurse

Job Summary
We are seeking a dedicated and energetic Part-Time Research Coordinator Infusion Nurse to join our dynamic clinical research team. In this role, you will be responsible for coordinating and executing infusion procedures within clinical trials, ensuring adherence to regulatory standards and maintaining high-quality patient care. This position offers an exciting opportunity to contribute to groundbreaking research while supporting patient safety and data integrity. The ideal candidate will possess strong nursing skills, clinical trial management experience, and a passion for advancing medical science through meticulous documentation and compliance.

Duties

• Administer infusion therapies to research participants in accordance with study protocols, ensuring precise adherence to dosage and timing instructions
• Monitor patients’ vital signs, responses, and overall well-being throughout the infusion process, promptly addressing any adverse reactions or complications
• Review and verify clinical trial documentation for accuracy, completeness, and compliance with FDA regulations and ICH GCP standards
• Collect blood samples via phlebotomy for laboratory analysis, ensuring proper technique and sample handling in line with clinical laboratory standards
• Maintain detailed records of patient interactions, infusion procedures, and observations within electronic medical record (EMR) systems while ensuring HIPAA compliance
• Coordinate with the research team to manage data collection, entry, and management using statistical software and CDISC standards for data consistency
• Supervise junior staff or volunteers involved in the trial process, providing guidance on protocol adherence and safety procedures

Skills

• Proven experience in nursing with a focus on infusion therapy, blood sampling, or related clinical procedures
• Strong understanding of clinical trials management, including protocol review, documentation review, and compliance management
• Excellent knowledge of medical terminology, HIPAA regulations, FDA guidelines, and ICH GCP certification standards
• Proficiency in using EMR systems, statistical software, and data management tools aligned with clinical research needs
• Skilled in patient monitoring techniques, vital signs assessment, and analysis skills to interpret clinical data accurately
• Ability to supervise staff or volunteers effectively while maintaining a collaborative team environment
• Familiarity with CDISC standards for data collection and reporting within clinical development projects

Join us in making a meaningful impact on healthcare through innovative research! We value proactive professionals who thrive in fast-paced environments and are committed to excellence in patient care and scientific integrity. This paid part-time position offers flexible scheduling options designed to fit your lifestyle while contributing to vital medical advancements.

Pay: $36.28 - $45.70 per hour

Benefits:

• Dental insurance
• Flexible schedule
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Education:

• High school or equivalent (Preferred)

Work Location: In person