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!
Join us at the Liberty Hotel in Boston, MA or online from Sunday, October 2 to Monday, October 3 to explore and help shape designs for the first therapeutic trials to pursue Parkinson’s disease prevention. View the agenda updated with new advocacy, regulatory, and industry perspectives. Virtual registration is open until October 2, 2022.
A limited number of in-person seats and hotel rooms for the night of October 2 are available. If you have not yet registered and would like to attend IN-PERSON, please email Katherine at email@example.com
All primary investigators on PSG studies must be credentialed, as well as sub-investigators.