The Research Nurse provides administrative and clinical support for Clinical Trials at the CCfV Challenge Unit. The Causal Relief Research Nurse is responsible for a wide range of duties including some or all of the following: research project logistics, conducting visits, and participant follow-up.
Requirements
- Review study protocol and orientation materials, attend study orientation meetings/site initiation visits
- Participate in study meetings, training, and maintain a current knowledge of the study status and important milestones
- Provide nursing care and support to clinical trial participants
- Educate participants about study procedures and requirements
- Administer investigational products and perform study-related procedures according to protocol and regulatory standards
- Accurately document study data, maintain source records, and ensure compliance with Good Clinical Practice (GCP)
- Collaborate with the research team to ensure smooth trial operations, including scheduling visits and coordinating with laboratory and clinical staff
- Monitor participant safety, promptly report adverse events, and follow safety protocols
- Maintain appropriate study blinding, randomization methods, and drug accountability records
- Maintain study documentation in adherence with the CCfV filing system
- Act as professional liaison with study participants
- Venipuncture will be required
Benefits
- Healthcare benefits
- Retirement plan
- Generous paid time off
- Wellness programs