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EPharma Global

EPharma Global

EPharma Global

Clinical Trial Administrator


Duration: 20 CPD Hours

 

The role of a Clinical Trial Administrator involves the following:

  • Assist Clinical Team Lead and Clinical Research Associates (CRAs) with accurately updating and maintaining clinical systems
  • Prepare, distribute, file and archive clinical documentation
  • Conduct periodic reviews of study files for completeness and accuracy
  • Act as a Central contact for the clinical team
  • Often assist in the set-up of investigator meetings
  • Assist the Clinical Research Associates or Lead CRA in site issues and management
  • May be involved in budgets and finance administration and preparing invoices
  • Often schedule and participate in vendor meetings where studies are outsourced
  • May accompany CRAs on site visits with the opportunity to experience clinical monitoring duties
  • Assist in orienting and training new staff

 

Course description:

This course is comprehensive and supports those seeking a position within the hospital/CRO/Biotech/Pharmaceutical Industry- it is possible to continue studying while employed in this industry (i.e towards degree level) while gaining excellent experience within the industry in parallel. This course is designed for those that have none or very little experience of in the field of clinical research (High school graduates or A Levels required as a minimum). Estimated completion time 20 hours on-line.

Elements covered in this course:

  • Good Clinical Practice
  • Essential Documents
  • Protocol, Investigators Brochure and Case Record Form
  • Regulatory Affairs
  • Ethics Committees & Submission process
  • In depth training for the role of Clinical Trial Administrator
  • Extensive training covering all tasks commonly assigned to the Clinical Trial Administrator.

Enrol for Critical Trial Administrator Training

CPD LogoREC Member

Pharmaceutical Training’ in Clinical Research for:
Science and Nursing graduates/post graduates to train as Clinical Research Associates (CRA), Clinical Project Managers (CPM), Pharmacovigilance Associates (Drug Safety) and to gain knowledge in Good Clinical Practice and Audit Preparation and Response