Jill Harper
About Jill Harper
Jill Harper is a Nurse Research Specialist currently working at the National Institutes of Health. She has extensive experience in clinical research, having held various positions in nursing and research across multiple institutions, including the University of Maryland Medical Center and Maryland Proton Treatment Center.
Work at National Institutes of Health
Currently, Jill Harper serves as a Nurse Research Specialist at the National Institutes of Health, a position she has held since 2023. In this role, she is involved in various research initiatives, contributing her expertise in nursing and clinical trials. Her responsibilities include coordinating and managing clinical research activities, particularly in the field of oncology.
Previous Experience in Nursing and Research
Jill Harper has a diverse background in nursing and clinical research. She worked as a Registered Nurse in the Medical Intensive Care Unit at the University of Maryland Medical Center from 2015 to 2016. Following this, she served as a Research Nurse Coordinator at the Maryland Proton Treatment Center from 2017 to 2019. Additionally, she held the position of Research Associate at the University of Maryland School of Medicine from 2008 to 2013 and worked as a Research Nurse at SNBL CPC for a brief period in 2016 to 2017.
Education and Expertise
Jill Harper has a strong academic background in the sciences and nursing. She earned her Ph.D. in Microbiology and Immunology from The Johns Hopkins University, completing her studies from 1999 to 2005. She also holds a Master of Science in Nursing with a focus on Clinical Nurse Leader from the University of Maryland School of Nursing, obtained in 2014. Additionally, she has a Master of Science in Biology from Indiana University Indianapolis, achieved in 1999, and a Bachelor of Arts in Spanish from Carleton College, completed in 1997.
Clinical Trials Coordination Experience
Jill Harper has extensive experience in coordinating clinical trials, particularly in oncology. She has worked on Phase 1 to Phase 3 clinical trials, managing both investigator-initiated and externally sponsored studies. Her expertise includes regulatory submissions and data entry, ensuring compliance with clinical trial protocols. She interacts with a diverse group of cancer patients, providing care and support throughout various stages of their treatment.