Quality Data...Delivered by Design™

Quality Data...Delivered by Design™



Webinar: Principal Investigator Training: Roles and Responsibilities


Course Title

Principal Investigator Training: Roles and Responsibilities


Date

This 2 hour webinar session is scheduled at the customer's convenience. Please call 585-381-1350 x246 to schedule.


Summary

This course teaches GCP, FDA and ICH requirements and how they pertain to everyday Investigator responsibilities while conducting clinical research. The course describes the core competencies that every Investigator needs to conduct compliant and high quality clinical research.


Recommended Attendance

  • Clinical Research Investigators
  • Clinical Research Coordinators
  • Monitors
  • Clinical Research Associates
  • Project Managers
  • GCP Auditors
  • Regulatory personnel

Instructor Bio

Lorraine D. Ellis, MS, MBA.
Ms. Ellis is an experienced trainer with in-depth knowledge as a result of hands-on experience in clinical trials and training thousands of clinical research professionals over decades. Ms. Ellis has over 30 years clinical research experience and is the author of several books, articles and other clinical research materials. She has authored and taught over 50 courses designed for clinical research professionals.

She has presented at major industry meetings such as DIA, ACRP, CRO Partnerships and others. Ellis has also served as faculty for ACRP courses, participated in the development of ACRP certification programs, and is an adjunct professor in the MS in Clinical Research Management program at Rochester Institute of Technology.


Cost

Call for our competitive pricing. Volume pricing and subscription pricing available.


To Register

Contact us at 585-381-1350 x246.