Webinars >>Clinical Trials Management
Workflow Management in Clinical Trial Projects: Learning from the FDA
Clinical trial are highly complex projects are that involve tens of processes covered by 100+ SOPs performed by large teams of individuals. Trial teams, big and small, struggle with optimizing their operations covered by SOPs. Project managers spend as much as 50-70% of their time chasing individuals to get updates, doing group meetings, writing long email trails, and creating reports that often contain redundant information. Much of the workflow is managed using manually created Excel worksheets or at best MS Project. This seminar, delivered by a leading clinical program manager, will highlight key areas where project managers can improve performance without sacrificing quality. This webinar will discuss, ways to use technology to automate tracking activities to reduce manual updates thereby increasing productivity and reducing waste. In a highly competitive clinical project management industry, increased productivity could translate into financial and regulatory rewards.
Why should you attend:
If you are managing or sponsoring a clinical trial, or plan to do so in the near future, this seminar will help you understand the limitations of commonly used practices to manage clinical trials, and ways to address the same. The webinar will discuss tools to track all functions including individual performance tracking, troubleshooting delays and non-compliance challenges. If you want to improve the efficiency of your quality systems, this webinar is for you. If you want to optimize your SOPs and evaluate efficiency tools you should attend this webinar. Case studies and automation tools will be presented.
Areas Covered in the Session:
Who will benefit:
For additional information on the workshop agenda and logistics, please call 410-501-5777 or email: firstname.lastname@example.org