Holly Orme
About Holly Orme
Holly Orme is a Senior Clinical Research Associate with over 20 years of experience in clinical research, specializing in various therapeutic areas. She currently works as an independent contractor, guiding clinical sites to ensure compliance and meet study milestones.
Work at Independent Contractor
Holly Orme has been serving as a Senior Clinical Research Associate at Independent Contractor since 2020. In this role, she employs efficient research study processes and strategies to support tracking, monitoring, compliance, documentation, and closure of clinical trials. Her responsibilities include guiding clinical sites from start-up to close-out, ensuring that they meet regulatory requirements, budgetary constraints, study milestones, and organizational goals.
Education and Expertise
Holly Orme has an extensive educational background in nursing and clinical research. She studied at Vanderbilt University, where she earned a Bachelor of Science in Clinical Research. Additionally, she completed a Bachelor of Science in Nursing (BSN) at Belmont University. She furthered her education at Walden University, where she studied Nursing Science and is currently pursuing a Master's Degree in Nursing, with only 5 credits remaining. Her academic training supports her over 20 years of experience in the clinical research field.
Background
Holly Orme has over 20 years of experience working with Contract Research Organizations (CROs), academic institutions, and pharmaceutical companies. Her expertise spans various therapeutic areas, including rare diseases, stem cell research, oncology, central nervous system (CNS) studies, and vaccine/infectious diseases. This diverse experience has equipped her with the skills necessary to navigate complex clinical research environments.
Achievements
Throughout her career, Holly Orme has demonstrated a commitment to ensuring clinical sites achieve compliance with International Council for Harmonisation (ICH), Good Clinical Practice (GCP), and ALCOA standards. She considers it a duty as a nurse to manage sites until they are fully compliant. Her thorough approach to clinical research has contributed to the successful execution of numerous clinical trials.