Clinical Research Nurse
Responsible for managing all aspects of conducting trials, clinical or otherwise; responsible for all aspects of the study to include recruitment, enrollment, ensure adherence to protocol, training of staff, completion of all study visits for eligible participants, GCP, FDA & OSHA regulations. Practiced nursing within the scope of Mississippi RN license to assess, diagnose, plan, implement, & evaluate the nursing care and treatment for the neuroscience patient population.
- Collaborated with investigators, directors, & sponsors to meet study objectives & resolve problems related to study budget, data, or activities
- Interacted with study sponsors, regulatory agencies & the IRB on behalf of the study
- Prepared IRB documents, progress reports, budget, and maintained the regulatory documents
- Managed data and maintained the research database to ensure confidentiality and data integrity