What are the responsibilities and job description for the Clinical Research Nurse Coordinator position at Northshore Research Associates LLC?
Job Overview
We are seeking a dedicated and highly organized Clinical Research Nurse Coordinator to join our dynamic research team. In this vital role, you will oversee the coordination and management of clinical trials, ensuring adherence to regulatory standards and ethical guidelines. Your expertise will facilitate seamless communication between research teams, healthcare providers, and participants while maintaining the highest quality standards in data collection, patient monitoring, and trial compliance. This position offers an exciting opportunity to contribute to groundbreaking medical research and improve patient outcomes through meticulous trial management and clinical excellence.
Duties
- Coordinate and oversee all aspects of clinical trials, including participant recruitment, enrollment, and follow-up procedures
- Monitor patient health status throughout the study, including vital signs, blood sampling, and adverse event documentation
- Review and ensure accuracy of clinical documentation in accordance with FDA regulations, ICH GCP guidelines, and healthcare compliance standards
- Conduct patient assessments, phlebotomy procedures, and blood sampling with precision and care
- Manage data collection and entry using EMR (Electronic Medical Record) systems and statistical software to support data integrity and analysis
- Supervise research staff and collaborate with multidisciplinary teams to ensure project milestones are met on time
- Maintain strict adherence to clinical ethical guidelines, HIPAA regulations, and clinical quality assurance standards throughout all trial activities
- Review clinical laboratory results and ensure proper documentation review for accuracy and compliance
- Facilitate training sessions on GCP (Good Clinical Practice), CDISC standards (Clinical Data Interchange Standards Consortium), and other research protocols
- Oversee project management tasks related to research project timelines, resource allocation, and compliance management
Experience
- Proven supervising experience in a clinical research or healthcare setting with leadership responsibilities
- Strong knowledge of medical terminology, clinical research methods, and healthcare compliance regulations including FDA regulations, HIPAA, and ICH GCP guidelines
- Experience with clinical laboratory procedures such as blood sampling and phlebotomy
- Proficiency in data management tools, EMR systems, Microsoft Office Suite, and statistical software for data analysis
- Familiarity with clinical trials management software and CDISC standards for data collection and reporting
- Certification in ICH GCP from a recognized issuer (e.g., ACRP or SOCRA) is required; valid LA RN license required.
- Background in nursing or healthcare with experience in research setting environments emphasizing clinical development and quality assurance standards
- Project management experience within healthcare or research projects demonstrating organizational skills and compliance oversight
- Ability to review complex documentation accurately while maintaining attention to detail in a fast-paced environment
Join us as a Clinical Research Nurse Coordinator where your expertise will directly impact innovative medical advancements. We value your dedication to excellence in clinical trials management—help us shape the future of healthcare through meticulous research practices!
Pay: $30.00 - $35.00 per hour
Expected hours: 20.0 – 30.0 per week
Work Location: In person
Salary : $30 - $35