Diligent research professional with strong background in clinical research and patient care. Managed complex clinical trials and contributed to groundbreaking studies. Demonstrated leadership in team coordination and protocol adherence, effectively utilizing critical thinking and problem-solving skills.
Overview
16
16
years of professional experience
1
1
Certification
Work History
Senior Research Nurse
MD Anderson Cancer Center
12.2015 - 09.2023
Manages multiple complex Phase 1 and 2 sponsor and IND clinical trials for acute Leukemia
Reviews medical records to screen potential patients for protocol eligibility
Assists the primary investigator with the consenting process following established standard of practice and good clinical practice guidelines
Assessed potential risks associated with trial participation, ensuring fully informed consent was obtained from all participants prior to enrollment.
Monitors and documents adverse events according to protocol requirements
Educates patients on all aspects of the clinical trial including side effects and risks, protocol compliance and protocol specific teaching
Creates detailed reports for principal investigators summarizing findings from research activities
Ensures compliance with applicable federal regulations by maintaining accurate records and preparing reports as needed
Collaborates with other healthcare providers to ensure the safety of participants in clinical studies
Establishes effective working relationships with sponsors and other research organizations involved in clinical studies
Enhanced data accuracy through diligent documentation of research findings and patient information.
Trained and mentored developing research nurses, providing guidance on best practices, ethical considerations, and research methodologies.
Advanced professional knowledge by participating in ongoing training opportunities related to emerging trends in healthcare research.
Senior Clinical Research Nurse
National Institutes of Health
02.2008 - 12.2015
Provided comprehensive clinical care to patients enrolled in diverse research protocols within the surgical oncology, medical oncology, and urology branches
Proficiently administered chemotherapy, biotherapy, cellular products, CAR-T therapy, and investigational agents to patients according to established protocols and physician orders
Monitored patients closely during treatments, promptly identifying and responding to any adverse reactions or side effects
Educated patients and their families about treatment plans, potential side effects, and self-care measures to improve treatment outcomes
Monitored participant health status during the duration of the study period
Monitored, recorded, and reported symptoms or changes in patients' conditions
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