With over 26 years of clinical trial experience, I have a deep understanding of the complexities involved in the oversight and conduct of research protocols while ensuring compliance with regulatory standards. In my various roles including CRC, CRA, CTM and Director, I have honed skills that are directly related to the successful implementation of site start-up strategies. I have successfully led multiple cross-functional teams from both the site and CRO perspective. This has allowed me to effectively strategize, allocate resources and streamline the start-up process. This experience has been within the US and has also included Global start-up strategies which involves rigorous oversight of regulatory requirements. Because of the recent experience of being both a Site Director and a CRO Director, I have a special insight into what has worked most effectively with the increasing complexity and expedited timelines of clinical trial start-up.

Session:

• A Site-Sponsor/CRO Team Approach to Clinical Trial Start-Up Strategies