The Clinical Research Nurse/Coordinator will be responsible for implementation and on-going management of clinical research trials in accordance with the code of federal regulations and Good Clinical Practices (GCP). Primary responsibilities will include interacting with patients and physicians, site preparations, screening and enrollment of research subjects, adherence to study protocols and ensuring necessary data is collected/reported in the appropriate source documents/CFR’s, assisting investigators with study subject visits, and accountability for test articles. This individual also serves as the primary contact between study site and sponsor/monitor organizations.
Qualifications and Other Required Knowledge and Skills:
- BS/BA with a healthcare related field with 5+ years experience and/or solid background in nursing - RN degree preferred
- Knowledge of Microsoft Office systems, especially MS Word and MS Excel
- Familiarity with GCP’s, Regulatory and Medical Monitoring Guidelines
- Excellent organizational skills. Able to execute multiple tasks in a fast-paced, changing environment, with ability to pay special attention to details