Purchase the recording of a web seminar you have attended in the past and SAVE 50%! Contact Barnett Customer Service for details: +1 781.972.5400 or toll-free in the U.S. at 800.856.2556.
Web Seminar Archives provided through Barnett’s Learning Management System (Single User access) or by electronic file transfer (Site License).
Site license archives are also available in SCORM format for LMS integration. Please contact Barnett at (215) 413-2471 for more details and pricing on SCORM files.
Bulk Archive access is available via Barnett’s Training Subscription. Click here to learn more.
Archive: Monitoring Oncology Clinical Trials
Course Description
This web seminar will provide attendees with a general overview of oncology clinical trials and their distinct characteristics. We will review how oncology clinical trials differ from those in other therapeutic areas, with a special emphasis on the unique challenges of monitoring oncology clinical trials. Distinctions will be drawn between early and later phase trials. Attention will be paid to Adverse Event (AE) and Serious Adverse Event (SAE) reporting. All aspects of oncology clinical trials and how to successfully monitor them will also be discussed.
Video Preview
Learning Objectives
- Identify the differences between monitoring oncology early phase clinical trials vs. later phase clinical trials
- Identify ways in which oncology clinical trials differ from those in other therapeutic areas
- Describe the complexities of AE and SAE monitoring in oncology clinical trials
- Utilize Common Terminology Criteria for Adverse Events (CTCAE) grading and apply CTCAE to AE source data
- Describe the common challenges in monitoring and apply tools and techniques to overcome them
Who Should Attend
- Monitors who are new to or are interested in learning more about oncology clinical trials
Instructor
Vanessa Laroche, B.S., CIP, CQA, C.C.R.P.
Click here for complete trainer biographies
Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.
