Clinical Research Nurse Coordinator

Job Summary
We are seeking a dedicated and energetic Clinical Research Nurse Coordinator to lead and manage clinical trials with precision and passion. In this vital role, you will coordinate patient care, ensure compliance with regulatory standards, and oversee data collection to support groundbreaking research initiatives. Your expertise will drive the success of clinical studies, ensuring they meet rigorous quality and safety standards while providing exceptional patient monitoring and support throughout the research process. Join us to make a meaningful impact on medical advancements and patient outcomes!

Duties

• Coordinate all aspects of clinical trial activities, including patient recruitment, enrollment, and follow-up care.
• Monitor patients closely during trials, recording vital signs, blood sampling, and other clinical assessments in accordance with protocol requirements.
• Review and verify documentation for accuracy, completeness, and compliance with FDA regulations, ICH GCP guidelines, and HIPAA standards.
• Manage data collection and entry using electronic medical record (EMR) systems and ensure adherence to CDISC standards for data management.
• Supervise research staff and collaborate with multidisciplinary teams to ensure seamless trial operations and compliance management.
• Conduct clinical laboratory procedures such as phlebotomy and blood sampling with precision and safety.
• Maintain detailed records of patient progress, adverse events, and protocol deviations while ensuring confidentiality at all times.
• Stay current on clinical development trends, regulatory updates, and best practices in clinical trials management to optimize trial success.

Experience

• Proven supervising experience in a clinical research setting or related healthcare environment.
• Extensive knowledge of clinical trials management, including FDA regulations, ICH GCP certification, and HIPAA compliance.
• Strong understanding of medical terminology, clinical laboratory procedures, and data collection techniques.
• Hands-on experience with EMR systems, statistical software for data analysis, and blood sampling procedures.
• Demonstrated ability to monitor patients effectively while maintaining high standards of safety and compliance.
• Familiarity with clinical development processes from early-phase trials through late-stage studies.
• Excellent analysis skills complemented by attention to detail in documentation review and data management tasks. Join us as a Clinical Research Nurse Coordinator to advance innovative medical research while providing exceptional patient care! Your expertise will help shape the future of healthcare through meticulous trial management, compassionate patient interaction, and unwavering commitment to excellence.

Pay: $25.00 - $37.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Vision insurance

Work Location: In person