CT: Nuts and Bolts of Monitoring Clinical Trials
FPM-40187
See the Site from the Sponsor's perspective: important for both monitors and coordinators. Topics include responsibilities of sponsors and investigators; qualifying investigators; regulatory document review; study initiation; routine monitoring tools, documents, and techniques; closeout visits; site management; and handling difficult situations.
Course Information
Course sessions
Section ID:
Class type:
This course is entirely web-based and to be completed asynchronously between the published course start and end dates. Synchronous attendance is NOT required.
You will have access to your online course on the published start date OR 1 business day after your enrollment is confirmed if you enroll on or after the published start date.
Textbooks:
No textbook required.
Policies:
Note:
Schedule:
Instructor: Jenny Paredes
Senior Manager, Clinical Operations, PRA Health Sciences
Senior Manager, Clinical Operations, PRA Health Sciences
Section ID:
Class type:
This course is entirely web-based and to be completed asynchronously between the published course start and end dates. Synchronous attendance is NOT required.
You will have access to your online course on the published start date OR 1 business day after your enrollment is confirmed if you enroll on or after the published start date.
Textbooks:
No textbook required.
Policies:
Note:
Schedule:
Instructor: Jenny Paredes
Senior Manager, Clinical Operations, PRA Health Sciences
