The MHRA GCP Guide (2012) 14.2 Quality Systems states:-
“..demonstrate that training has occurred, documentation must2 be maintained and retained for all staff ….. The extent and content of this documentation is a business decision, but typically includes:
• a current job description dated and signed by the post-holder and their line manager to demonstrate the date on which current roles and responsibilities have been agreed
• a curriculum vitae to demonstrate current and previous relevant education and experience, signed and dated to confirm the date of the document and ownership by the named individual
• confirmation that GCP training has taken place (including clear reference to the framework used in the training, such as, Statutory Instruments, EU Directives)
• role-specific training relevant to the post-holder’s duties &trial role(s)
• written procedure training records”

The word “Typically” is not a MHRA codified word, such as "must" and "should". It may mean that it is good practice?


Reference:- Must2 = Reg31A.(4) The essential documents relating to a clinical trial are those which—(a) enable both the conduct of the clinical trial and the quality of the data produced to be evaluated