Feeling stressed from managing clinical trials? Do you want to take control and be in charge?
Then this course is for you.
This two-day seminar, worth 12 contact hours, provides an overview of the different project management approaches used by Sponsors and Contract Research Organizations, and helps you decide how to apply them in your situation. Your course developer and trainer has 16 years of experience in the pharmaceutical and contract research industries, so the course is specifically designed for clinical research project management, with examples and exercises developed using pharmaceutical research scenarios. A key component to this course is that you will learn how to take real control of your clinical trials, to actually manage and direct them, rather than simply tracking what is happening. Enrollment is limited to 40 participants.
By the end of the course, attendees should be able to:
This course is for clinical research professionals, both those who directly manage clinical trials and those working through other organizations such as CROs. Whether you have a clinical role as a Clinical Research Associate (CRA), Clinical Study Manager, Project Manager or Director-level position, this two-day program will provide you with the intensive training needed to improve your project management skills. Attendees new to project management will receive an introduction to the project management of clinical trials, whereas those more familiar with project management will receive a boost to their knowledge and further their understanding of how Sponsor and CRO companies operate.