Brittany Nash

Provided immediate post-operative care, ensuring patient stability and comfort after anesthesia.
Worked closely with healthcare professionals to deliver patient-centered services.
Evaluated vital signs and pain levels, addressing issues swiftly during recovery.
Developed strategies to manage complications arising in post-anesthesia scenarios.
Facilitated effective communication with patients and families regarding care procedures.
Adapted to dynamic clinical environment by exercising critical thinking skills.
Managed multiple tasks simultaneously while upholding quality patient care standards.
Exhibited commitment to nursing excellence through ongoing professional development.

• Administered medications and treatments as prescribed by healthcare providers.
• Assisted in patient assessments and documented health information accurately.
• Educated patients on health management and self-care techniques.
• Collaborated with multidisciplinary teams to enhance patient care strategies.
• Maintained cleanliness and organization of medical equipment and supplies.
• Participated in training new staff to ensure compliance with healthcare standards.
• Administered medications and treatments according to established protocols.
• Performed physical assessments, including vital signs and health history documentation.
• Maintained a safe environment by following infection control policies and procedures.
• Administered prescribed medications or started intravenous fluids, noting times and amounts on patient charts.

• Coordinated patient recruitment and enrollment for clinical trials in renal care.
• Managed regulatory submissions and documentation for study compliance.
• Collaborated with healthcare teams to ensure protocol adherence in studies.
• Organized training sessions for staff on clinical research procedures.
• Monitored patient data collection and maintained accurate records.
• Implemented standard operating procedures for clinical trial operations.
• Facilitated communication between sponsors and study sites to resolve issues.
• Led site visits to assess compliance with study protocols and regulations.
• Communicated effectively with investigators, study staff, sponsors, vendors, IRB personnel, and other stakeholders throughout the life cycle of the trial.
• Maintained accurate up-to-date tracking logs for all aspects of clinical research activities including but not limited to adverse events, serious adverse events, concomitant medications, lab results .