CT: Site and Investigator Recruitment
FPM-40208
This course is intended to help a clinical study sponsor recruit the appropriate sites and investigators for the study. Topics include sources of information on sites and investigators; approaching and evaluating the potential investigator and the potential site; and understanding the application of good clinical practices.
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:
Jan Agee, B.S., CCRA
Training Manager and Instructor for Quintiles in San Diego
Jan Agee is a clinical trials consultant currently assisting an academic institution organization in conducting Food and Drug Administration-focused clinical trials. With over 30 years of industry experience, Agee has expertise in pre-clinical and clinical drug and device development.
Her background includes clinical operations implementation across all phases of drug development, good clinical practice training and implementation. Her previous position was with a global contract research organization where she taught good clinical practices to new and experienced clinical, project management, medical and regulatory staff. Agee's prior experience also includes more than 13 years as a clinical research monitor (CRA) for numerous pharmaceutical companies across indications.
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:
Jan Agee, B.S., CCRA
Training Manager and Instructor for Quintiles in San Diego
Jan Agee is a clinical trials consultant currently assisting an academic institution organization in conducting Food and Drug Administration-focused clinical trials. With over 30 years of industry experience, Agee has expertise in pre-clinical and clinical drug and device development.
Her background includes clinical operations implementation across all phases of drug development, good clinical practice training and implementation. Her previous position was with a global contract research organization where she taught good clinical practices to new and experienced clinical, project management, medical and regulatory staff. Agee's prior experience also includes more than 13 years as a clinical research monitor (CRA) for numerous pharmaceutical companies across indications.
