Clinical Research Coordinator RN

4 days ago


ValdeReuil, Normandie, United States Novant Health Full time
Job Summary

The Clinical Research Coordinator RN is a key member of the research team at Novant Health, responsible for facilitating and coordinating daily clinical trial activities. This role plays a critical part in the conduct of studies, ensuring that all aspects of clinical research are executed with excellence, ethics, safety, quality, compliance, and stewardship.

At Novant Health, we value diversity and inclusion, and we invite applicants from all backgrounds to join our team. As a Clinical Research Coordinator RN, you will have the opportunity to work with a talented team of professionals who are dedicated to providing remarkable healthcare to our patients, families, and communities.

Responsibilities

The successful candidate will be responsible for:
  • Coordinating and facilitating daily clinical trial activities, including patient recruitment, informed consent, and data collection.
  • Ensuring compliance with regulatory requirements, including GCP, IATA, and human subjects training.
  • Collaborating with the research team to develop and implement study protocols, including clinical trial design, patient selection, and data analysis.
  • Providing excellent communication and interpersonal skills, including working with patients, families, and healthcare professionals.
  • Maintaining accurate and detailed records, including study documentation, patient information, and research data.
  • Participating in ongoing education and training to stay up-to-date with the latest research methods, technologies, and best practices.
Requirements

To be successful in this role, you will need:
  • A current RN licensure in the appropriate state.
  • A minimum of 1 year of nursing or clinical research experience.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and as part of a team.
  • Strong organizational and time management skills.
  • Ability to maintain confidentiality and handle sensitive information.
Preferred Qualifications

A clinical research certification, good clinical practice (GCP) training, and international air transportation association (IATA) certification for shipping hazardous and biological substances are preferred.

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