Monitoring Skills Training for the Non-Commercials (for the UK sector) 

This two-day course will provide an introduction to the skills required for monitoring research in the UK non-commercial sector. The course will focus on monitoring of clinical research trials of medicinal products. The course is designed for all staff involved in monitoring, or supervising monitoring of clinical research e.g.  R&D Managers, research governance staff, study coordinators, and investigator site staff. Enrolment is limited to 30 participants per course.

Who is Organising this Event?

The Association of Clinical Research Professionals in collaboration with the NHS R&D Forum.

Course Objectives

Upon successful completion of this course, participants should be able to:Understand the purpose and scope of monitoring

  1. Understand the purpose and scope of monitoring
  2. Be familiar with the Good Clinical Practice and UK regulations of clinical research
  3. Be familiar with the life cycle of a clinical research project of a medicinal product
  4. Understand the responsibilities of individuals associated with monitoring activities
  5. Be able to perform essential skills required for monitors
  6. Be able to write effective monitoring reports and identify the follow up actions

Download the course agenda (.pdf).

Upcoming Dates & Locations

The two-day course will be repeated about every two months thereafter in different parts of the UK, to enable delegates to attend a local course.

  • Wed 16th to Thur 17th July 2008, London (view map to location)
  • Tues 22nd to Wed 23rd July 2008, Nottingham
  • Sep 08 , dates TBC, Birmingham
  • Nov 08, (Host and venue TBC)
  • Dec 08, dates TBC, Oxford
  • 2009 (Hosts waiting TBC)

Registration

  • Costs £395 per person for 2 day course. 
  • If you interested in hosting the event to save travel and accommodation costs pleasecontact siobhan@acrpnet.org for further details).

Registration will be through the NHS R&D Forum. Please click here.

Contact

For further information on the course and to provisionally reserve a place on future training dates when they are released please contact:

Siobhan Lim RN, BSc,CCRC
Manager Clinical Research Training, ACRP
European Office, Windsor
Email: siobhan@acrpnet.org    Tel: 00 44 1753 831 908

Resources

You Might Be Interested In...

  • Two-Day Good Clinical Practice - Arlington

    Good Clinical Practices for Clinical Research Professionals is an intensive training course designed to boost knowledge and understanding of good clinical practices and locally applicable regulations and guidelines such as the FDA Code of Federal Regulations (CFR), the European Directives, and the International Conference on Harmonisation (ICH).
  • Education

    ACRP offers the training needed to be successful in clinical research today. View classroom courses, online learning options, webinars and Home Study tests from The Monitor.