Implementing Site-Centric Technology to Effectively Manage Your Clinical Trials
For academic medical centers and cancer centers, new technology can provide a foundation to streamline operations and reach your full research potential. Adopting a new clinical trial management system (CTMS) alongside additional operational and clinical solutions can help gain visibility into your research, boost compliance, manage your data, and much more. While these systems can bring immense value on their own, they become even more powerful when integrated with each other, and to the enterprise technology you’re already using.
This webinar will provide an overview of the benefits of adopting new clinical research technologies (focusing primarily on a CTMS), outline how to choose which systems are best for your organization, and share best practices for implementing those systems. Members of Advarra’s product management, sales, and project management teams will share their experience and insight into what research sites need to do to take their operations to a new level.
- Understand what technology capabilities are most important for academic medical centers and cancer centers, and where sites can see the most return on investment
- Learn what to look for when evaluating clinical trial management systems, eRegulatory systems, eConsent solutions, and more
- Hear how focusing on key goals during your implementation will help you see value from your system quicker, and how building a great team can help ensure the long-term success of your system and your operations
Director, Product Management
Senior Account Executive
Who should watch?
This content applies to research professionals involved in conducting clinical trials, including representatives from academic medical centers, cancer centers, and health systems managing a large volume of research.
The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit.
If you would like to obtain CE credits for a different credential, please check with your professional organization to determine if our webinars meet their continuing education requirements.
Certificate of Attendance
After watching this webinar in its entirety and completing the webinar survey, you will receive a certificate of attendance. This certificate will be emailed to you within one business day of watching the webinar. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and complete the webinar survey. Visit our Webinar Help page for more information on certificates of attendance.
DATE: October 19, 2021
Time: 1 pm ET | 10 am PT
Duration: 1 hour