Clinical Research Monitoring is an evolving practice. The purpose of this 4-day workshop is to assist Research Site Coordinators, Quality Assurance Auditors, and CRAs/Monitors in improving their skills and their understanding of the roles and responsibilities of the Clinical Research Associate/Monitor. Although designed with all research professionals in mind, this program is ideal for Research Study Coordinators who want to improve the understanding of their responsibilities and interactions with their Clinical Research Monitors, and for Monitors/Auditors/Project Managers with 0-5 years monitoring experience who want to increase their knowledge and understanding of monitoring responsibilities.
This interactive virtual workshop will be facilitated by clinical research professionals with a combined industry experience of more than 40 years. Information will be presented and discussed regarding monitoring clinical trials according to FDA Regulations and International Council for Harmonisation (ICH) guidelines as well as practical procedures and site / sponsor / CRO relationships.
Please note, this workshop is intended to be highly interactive. Video attendance is strongly encouraged. Once you register, you will be able to install and test the appropriate software to ensure your audio and video will work properly during the program. Please be sure to give yourself time to address any technical issues that might arise. Please contact us with any questions or concerns at email@example.com.
11:00 am to 3:00 pm ET*
*All times in Eastern Standard Time Zone
Member Fee- $435
Non-Member Fee- $510
Non-Member Fees include a non-refundable one-year membership in SOCRA