Dedicated Registered Nurse with 23 years of extensive clinical and leadership experience, focused on driving transformative change within healthcare systems. Exceptional analytical, communication, and teamwork skills are complemented by a proven track record of adapting swiftly to dynamic environments. Committed to fostering team success while actively pursuing professional development opportunities. A positive attitude and unwavering dedication to continuous learning support a strong desire to enhance patient care and contribute meaningfully to the healthcare community.
Achieved an 80% increase in staff retention since assuming a managerial role in 2024 by fostering a supportive, growth-oriented work culture.
Expanded continuing education offerings to address emerging healthcare trends and meet the diverse learning needs of clinical staff.
Developed, implemented, and continuously evaluated orientation programs, in-service training, and continuing education initiatives for nursing personnel, enhancing clinical competency and compliance.
Oversaw hospital-wide education initiatives, promoting evidence-based practice and ensuring high-quality, safe patient care through targeted educational interventions.
Integrated simulation-based learning into clinical curricula to better prepare nursing staff and students for real-world challenges in patient care.
Improved accreditation outcomes by aligning educational programs with national standards and clinical best practices, contributing to institutional excellence.
Administered medications via oral, intravenous (IV), and intramuscular (IM) routes; monitored therapeutic and adverse responses for up to six patients concurrently, ensuring safety and efficacy.
Performed complex wound care, including daily VAC (Vacuum-Assisted Closure) and PICO dressing changes, promoting optimal healing outcomes.
Maintained accurate and timely documentation for 4–6 patients per shift, including comprehensive assessments, nursing interventions, and patient outcomes in full compliance with regulatory and institutional standards.
Remained calm and effective during high-stress and emergency situations, providing critical care support during code blues, rapid responses, and disaster scenarios.
Conducted study visits and ensured full compliance with ICH/GCP guidelines and FDA regulations, maintaining high standards of clinical research integrity and participant safety.
Successfully managed six or more concurrent clinical trials, demonstrating strong organizational and multitasking abilities in a fast-paced research environment.
Drafted and revised informed consent forms, served as the primary liaison with Institutional Review Boards (IRBs)/Ethics Committees, and coordinated with pharmaceutical sponsors to ensure regulatory and procedural alignment.
Participated in Investigator Meetings for new study initiations, gaining in-depth knowledge of investigational products and protocols to effectively train and educate site staff.
Rajchgot, Jason MD*; Siemieniuk, Reed A. C. MD*,†; Sivachandran, Nirojini MD, PhD*; Murphy, Pauline RN‡; Sharp, Andrea MSW‡; Cicci, Angela RN‡; Bogoch, Isaac I. MD*,‡,§Author Information
JAIDS Journal of Acquired Immune Deficiency Syndromes 72(3):p e80-e81, July 1, 2016. | DOI: 10.1097/QAI.0000000000001004