Clinical Research Coordinator

2 weeks ago


Neenah, Wisconsin, United States Radiant Systems Inc Full time

Position Overview: A Clinical Research Coordinator at Radiant Systems Inc. is a dedicated professional responsible for managing and supervising the clinical operations of research initiatives. This role involves assessing and ensuring the safety of study participants while adhering to established clinical research guidelines and protocols.

Key Responsibilities:

  • Review and evaluate records to identify potential research participants; maintain comprehensive study documentation in accordance with sponsor protocols.
  • Screen clinical study candidates for eligibility; schedule and conduct interviews to assess suitability.
  • Provide education to potential participants and their families, as well as to nursing and ancillary staff regarding study procedures, treatments, and potential side effects.
  • Facilitate informed consent processes, ensuring participants understand the protocol and their rights.
  • Assist in creating educational materials for participants and their families, providing guidance on study-related procedures.
  • Conduct nursing assessments and monitor participant progress throughout the study, promptly reporting any adverse events to the Principal Investigator or Clinical Research Manager.
  • Conduct initial interviews during participant visits and implement appropriate procedures as outlined in the study protocol.
  • Set up and verify any required instrumentation for the study, ensuring accurate data collection.
  • Troubleshoot basic equipment issues as needed.
  • Coordinate all research activities and procedures for study participants.
  • Complete case report forms for each participant and maintain accurate study data records.
  • Monitor and document participant compliance with study protocols.
  • Provide training and support for new and existing personnel involved in research activities, participating in staff meetings and educational sessions.
  • Manage inventory of necessary research supplies and maintain laboratory and examination areas.

Qualifications:

  • Licensed healthcare professional, such as RN, LPN, or radiological technologist.
  • Preferred: One year of experience in a clinical research environment.

Exceptional communication skills, a strong sense of empathy for participants, and the ability to work independently are essential. Candidates should possess robust problem-solving skills and a solid understanding of OSHA guidelines for handling hazardous materials.



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