Clinical Research Nurse at Arch Clinical Trials in St. Louis, MO

Job Overview

We are seeking a dedicated and 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 and ethical guidelines. Your expertise will support the advancement of innovative medical treatments by managing patient care, collecting high-quality data, and maintaining compliance with industry regulations such as FDA, ICH GCP, and HIPAA. This position offers an exciting opportunity to contribute directly to groundbreaking research while fostering a collaborative and patient-centered environment.

Duties

• Available 7-330pm and 3-1130pm Shift- able to rotate on weekends if needed
• Monitor and assess patient health status throughout clinical trials, including vital signs, blood sampling, and other clinical assessments
• Supervise clinical staff to ensure proper protocol adherence and data collection procedures
• Review documentation for accuracy, completeness, and compliance with regulatory standards
• Coordinate patient recruitment, informed consent processes, and retention strategies in accordance with ethical guidelines
• Manage data collection, entry, and management using statistical software and CDISC standards to ensure data integrity
• Conduct clinical laboratory procedures such as phlebotomy and blood sampling with precision and safety
• Ensure all activities comply with FDA regulations, ICH GCP guidelines, healthcare compliance standards, and clinical quality assurance protocols
• Available 7-330pm and 3-1130pm Shift- able to rotate on weekends if needed

Qualifications

• Proven supervising experience within a clinical research or healthcare setting
• Strong knowledge of medical terminology, clinical research methods, and regulatory requirements including FDA regulations, ICH GCP certification, and HIPAA compliance
• Experience with clinical trials management systems, data management tools, Microsoft Office Suite, and statistical software
• Clinical laboratory experience with phlebotomy, blood sampling, vital signs measurement, and analysis skills
• Familiarity with CDISC standards for data collection and analysis in research settings
• Excellent project management skills with the ability to coordinate multiple tasks efficiently in a fast-paced environment
• Valid certification in Good Clinical Practice (GCP) from an authorized issuer for CA or equivalent jurisdiction; additional certifications in clinical ethical guidelines are preferred
• Strong understanding of healthcare compliance standards related to clinical research and project management experience in healthcare environments

Join us to be part of a passionate team committed to advancing medical science through meticulous research practices. Your expertise will help shape the future of healthcare while ensuring the highest standards of patient safety and data integrity.

Pay: $23.00 - $32.00 per hour

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible schedule
• Life insurance
• Paid time off
• Retirement plan
• Vision insurance

Work Location: In person