Join the PSG for a 1-hour webinar about career opportunities and growth in the world of PD clinical research, with a focus on the role of the clinical research coordinator.
The PSG was thrilled to host Denise & Bernard Coley at our last Coordinator Webinar. Denise is the founder of Enable Your Vision, a firm that provides supplier diversity consulting to drive economic vitality for diverse businesses, corporations and the communities in which they reside. Bernard is an executive with 50+ years of experience in the high tech industry. He is also a Principal in Enable Your Vision. Since being diagnosed with Parkinson’s disease in 2018, Denise has been driven to increase Parkinson’s awareness, education, and communications to under-engaged and remote global communities with the support of her husband, Bernard. Together, they have been a part of the Parkinson’s Foundation’s Research Advocates Group and members of the Parkinson’s Foundation California Advisory Board. They have also done work with other PD organizations, such as the World Parkinson Congress and the PD Avengers.
Currently, Mr. Coley is aiming his talents and time in support of those interested improving the lives of individuals and families impacted by Parkinson’s disease. He is a member of the Parkinson’s Foundation’s Research Advocates group and an advisory board member of the California chapter of the Parkinson’s Foundation. And finally, he is joining his wife, Denise in an outreach initiative to increase awareness of PD and PD resources in underserved communities of color. They co-chair a special interest group focused on bringing Black perspectives to PD research.
Please note that due to technical difficulties, the first five minutes of the webinar were not included in the recording.
As a Senior Project Manager and Regulatory Document Specialist at the Center for Health + Technology (CHeT), Becky has been involved in and responsible for the management and health of the Trial Master Files (TMF) for many multi-site studies in the field of therapeutic clinical research. Working closely with site staff, monitors, sponsors, and study team members, Becky serves as a Subject Matter Expert (SME) for the regulatory aspects of a study. Within CHeT, Becky also serves as a leading member of the Regulatory Management Group, and serves as an SME for electronic TMF (eTMF) systems.