Job Summary
We are seeking a dedicated and energetic Clinical Research Nurse Coordinator to lead and manage clinical trial activities within our research team. This vital role involves coordinating patient care, ensuring compliance with regulatory standards, and overseeing the integrity of data collection throughout the clinical trial process. The ideal candidate will possess a strong background in nursing, clinical trials management, and regulatory compliance, with a passion for advancing medical research through meticulous coordination and patient-centered care. Join us to contribute to groundbreaking research that improves health outcomes worldwide!
Responsibilities
- Coordinate all aspects of clinical trial activities, including patient recruitment, enrollment, and follow-up care.
- Monitor patient safety and well-being throughout the trial, ensuring adherence to protocols and timely documentation of vital signs, blood sampling, and other clinical data.
- Review and verify study documentation for accuracy, completeness, and compliance with FDA regulations and ICH GCP standards.
- Manage data collection processes using electronic medical record (EMR) and EDC systems .
- Supervise clinical staff involved in trials, providing guidance on protocol adherence, documentation review, and compliance management.
- Conduct patient assessments, including vital signs measurement, blood sampling (phlebotomy), and monitoring for adverse events.
- Ensure all trial activities comply with HIPAA regulations to protect patient privacy and confidentiality.
- Collaborate with research teams to prepare reports, assist in statistical analysis using appropriate software, and support regulatory submissions.
Requirements
- Valid nursing license with current registration; certification in Good Clinical Practice (GCP) from an approved issuer is required.
- Strong understanding of medical terminology, clinical laboratory procedures, blood sampling techniques, and vital signs assessment.
- Experience with EMR systems, data management tools, statistical software, and compliance documentation review.
- Clinical laboratory experience or background in clinical development is highly desirable.
- Excellent analysis skills with attention to detail for data collection and documentation review.
- Ability to navigate complex regulatory environments such as HIPAA compliance requirements. Join our team as a Clinical Research Nurse Coordinator to be at the forefront of innovative healthcare solutions! Your expertise will directly impact the success of critical research projects while fostering a collaborative environment dedicated to excellence in clinical trials management. We are committed to supporting your professional growth through ongoing training opportunities and a dynamic work environment focused on making a difference in patients’ lives!
Pay: $25.00 - $35.00 per hour
Work Location: In person