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.
The PSG is looking to further enhance our research portfolio and as of late, increased opportunities have arisen for us to interact with industry. We are looking for motivated clinical trialists & statisticians who would like to learn more about these opportunities and grow with the PSG. If you are interested in learning more about how the PSG interacts with industry, or how to become more involved, please join our webinar on November 15, 2022 at 3:00 PM EST. Please note that junior level faculty are welcome to attend. Part of the PSG’s mission centers around training clinicians in the PD field and that is inclusive of our work with industry.
*Registration is coming soon!
All primary investigators on PSG studies must be credentialed, as well as sub-investigators.