This one-day course will look at the practical application of clinical research competencies as they relate to the role of the principal investigator and site staff. Through lecture, case examples and interactive exercises this course will focus on both the “WHY BEHIND” and the “HOW TO TRANSLATE” regulatory requirements into more efficient clinical trial conduct. By leveraging the competency requirements of clinical research coordinators and other research staff, participants will learn how to be more efficient in delegating responsibilities so that they are more effective as well as compliant in performing their duties as a Principal Investigator.
At the end of this session the participants should be able to:
This course is approved for 7.0 CME hours. No ACRP contact hours are offered.