Clinical Research Nurse

Overview

Energetic Clinical Research Nurse to join our dynamic research team. In this vital role, you will coordinate and oversee clinical trials, ensuring adherence to regulatory standards while providing exceptional patient care. Your expertise will help advance medical knowledge and improve patient outcomes through meticulous trial management and compassionate patient monitoring. This position offers an exciting opportunity to be at the forefront of clinical development, working within a collaborative environment committed to excellence and innovation.

Duties

• Manage and supervise clinical trial activities, including participant recruitment, enrollment, and follow-up procedures
• Conduct comprehensive patient assessments, including vital signs, blood sampling, and monitoring of clinical laboratory results
• Review and ensure accuracy of study documentation, including consent forms, case report forms, and regulatory compliance records
• Monitor patient safety throughout the trial process, promptly addressing adverse events and ensuring compliance with FDA regulations and ICH GCP standards
• Coordinate with multidisciplinary teams to facilitate data collection, data management, and analysis using statistical software and CDISC standards
• Oversee clinical laboratory procedures such as blood sampling and processing in accordance with protocol requirements
• Maintain detailed records within EMR (Electronic Medical Record) systems while ensuring HIPAA compliance for patient confidentiality
• Provide training and supervision to junior staff or research assistants involved in clinical trials management
• Ensure adherence to all regulatory guidelines related to clinical trials, including FDA regulations, ICH GCP certification requirements, and local compliance standards

Qualifications

• Registered Nurse (RN) license with current licensure in the applicable jurisdiction
• Proven supervising experience within a clinical research setting or healthcare environment
• Experience with clinical laboratory procedures such as phlebotomy and blood sampling
• Familiarity with EMR systems, data collection tools, and statistical software used in research analysis
• Excellent understanding of medical terminology, patient monitoring techniques, and vital signs assessment
• Demonstrated ability to review complex documentation for accuracy and regulatory compliance
• Knowledge of HIPAA regulations related to patient privacy and data security
• Strong analysis skills with attention to detail for data management and research documentation

Join us in advancing healthcare through innovative clinical research! We are committed to fostering a supportive environment where your expertise makes a meaningful impact on patient lives while offering opportunities for professional growth!

Pay: From $40.00 per hour

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Work Location: In person