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Clinical Research Nurse/Clinical Trials Coordinator

2 months ago

Mt Pleasant, South Carolina, United States Central Michigan University Full time
Job Summary

This position is a key member of the research team at Central Michigan University, responsible for managing clinical trials and ensuring compliance with regulatory requirements. The successful candidate will have a strong background in nursing and experience in clinical research.

Key Responsibilities
  • Manage clinical trials from initiation to completion, ensuring compliance with federal, state, and local regulations.
  • Develop and implement operational plans for clinical trials, including selection of patients, treatment procedures, and data collection.
  • Act as a liaison between hospital physicians and principal investigators, ensuring effective communication and collaboration.
  • Recruit and consent study patients, establishing a patient/coordinator relationship and ensuring patient safety.
  • Coordinate all aspects of research study exercises, including case report forms, patient visits, and query resolution.
  • Assess patients for consenting into clinical trials based on inclusion/exclusion criteria and execute study visits.
  • Prepare documentation as required by the study sponsor and/or principal investigator.
  • Train study patients under the direction of the principal investigator.
Requirements
  • Graduation from an accredited school of nursing.
  • Current registration with the State of Michigan Board of Nursing as a Registered Nurse (RN).
  • Certificate of completion for CITI training or willingness to obtain certification.
  • One year nursing experience related to the duties of the position.
  • Strong interpersonal and communication skills.
  • Ability to analyze and interpret data and maintain confidentiality.