Description

Clinical Operations Courses

During this half day training you will learn about the importance of the involvement of Clinical Operations in the review process for clinical study protocols with emphasis on how to do the review and how it can be optimised.

If you combine this course with GMP Essentials for Clinical Operations Staff and Clinical Project Management, you will get a reduction of 25% on both half-day courses.

During this half day training you will learn about the importance of the involvement of Clinical Operations in the review process for clinical study protocols with emphasis on how to do the review and how it can be optimised.

Course time
13h30 - 17h00
Who should attend

Clinical Operations Staff that is required to review critically study protocols before their finalisation. 

Programme highlights
  • Reviewer roles.
  • Common problems in the review process of clinical study protocols.
  • What makes a good review process?
  • Exercise on clinical study protocol review. 
Learning Objectives
  • Making the clinical study protocol review process work.
  • Optimizing the review process for clinical study protocols.

 

Competencies

This course covers competencies that are part of the ECCRT Competency Framework

  • Scientific Concepts & Research Design (5)
  • Ethical & Participants Safety Considerations (4)
  • Investigational Product Development and Regulation (1)
  • Clinical Studies Operations (GCPs or ISO 14155) (0)
  • Study and Site Management (0)
  • Data Management and Informatics (0)
  • Leadership and Professionalism (5)
  • Communication (0)
  • Teamwork (3)
  • Business acumen (0)

 

Be aware that attending one of ECCRT open course does not guarantee that the competency is acquired but only guarantees that the related knowledge has been trained 

Book a course

Date Lang Location
 
Proceeding your application may take up to 24 working hours. In case of question, contact campus@eccrt.com.
400,00 € excl. VAT (if applicable)