The Importance of Early Patient Involvement in Clinical Trial Design
Patient-centricity gets a lot of buzz, but what are the benefits of involving patients in the planning of a clinical trial? This webinar looks at:
- Where in the process to get patient input—from protocol reviews to endpoint selection to assessments
- How patient input can benefit enrollment, compliance, and outcomes
- What tactics can be used to elicit meaningful input
Jamie Arnott, R.N.
Senior Project Director
Jamie Arnott has been conducting clinical studies for more than 20 years in a broad range of therapeutic areas, focusing on rare disease studies since at Rho. Jamie has provided oversight and full management support for over 10 rare disease studies, including three U.S. and global programs. Ms. Arnott’s rare disease experience, including cystic fibrosis research, has included treatment with oral therapy, as well as aerosolized treatment and subcutaneous injections. These studies ranged from Phase 1 to 3 and have included inpatient components, telephone visits/assessments, serial PK collections, and quality of life assessments. Jamie has extensive experience from both the…
Senior Learning and Performance Specialist
Ryan Bailey is a Senior Learning & Performance Specialist at Rho. He has 15 years of experience in clinical research. His background and experience span a wide range of specialties, including: project management, business analysis, process improvement, and organizational development. In his current role, Ryan oversees corporate communication and change management initiatives.
Samantha Hoopes, Ph.D.
Dr. Hoopes has over 13 years of clinical research experience across a variety of biological, clinical, and regulatory fields. She works with companies at all stages of development to support their product development plans, clinical study design and execution, and management of clinical studies or regulatory submissions. She has led teams for regulatory submission programs and clinical studies from initiation through completion in a variety of therapeutic areas. She has extensive experience in scientific authoring and editing, including preparation of clinical study protocols, modules of regulatory submissions (NDA, IND, etc.), briefing packages, clinical study reports, informed consent documents, and other regulatory…