Learn the Ins-and-Outs of Study Management, the Clinical Study Environment, and overall Drug Development.
The success of a clinical study is very much dependant on its efficient preparation and effective conduct.
Study managers should be knowledgeable about required quality and regulatory standards, roles and responsibilities of team members, and be able to select and oversee internal and external resources.
Study managers also should be able to anticipate potential problems, offer creative solutions and develop strategies to mitigate risk.
This training course provides a comprehensive overview of the essential elements of study management and the clinical study environment in the context of the overall drug development process.
After successful completion of the training course, participants will be able to plan, execute and manage a clinical study from protocol to final report.
Member Industry : 1840
Non-Member Industry : 1970
Member Academia/Charitable/Government/Non-profit (Full-time): 920
Non-Member Academia/Charitable/Government/Non-profit (Full-time): 1050
Speakers: Patricia Fitzgerald, Nancy Hoffer, Päivi Itkonen, Angelika Karwoth, Jennifer Kealy, Tamara Schärer
+41 61 225 5151