Our Clinical Research Associates (CRAs)
are one of the strongest links in the chain and act as the
main line of communication between investigators and your
departments. While always ensuring subjects' wellbeing and
rights and data reliability, they promote and uphold the image
and values of your company at all times. Their professionalism
and enthusiasm is second to none in the market.
We offer our CRAs a comprehensive internal and external training
program featuring Standard Operating Procedures (SOPs), Good
Clinical Practice (GCP) and regulatory requirements. In addition,
they receive project specific training before the start of
any projects.
All monitoring activities are conducted according to the international
standards of ICH/GCP.
With the support of their Project Manager and Line Manager,
our CRAs are accountable for:
Investigational site identification
and qualification
Collection, review and tracking of
essential documents
