Compile, submit and maintain Health Authority (MCC) clinical
trial applications (CTA) Assist investigators
in preparation of Ethics submissions Comply with Adverse
Event reporting obligations
Every CTA is compiled or overseen by a Project Manager and critically
reviewed by a second senior colleague prior to submission. We
currently have a 94% record of MCC approvals on first review.
Selection and training of competent sites and investigators
is of critical importance. Triclinium maintains a database of
known investigators. If you would like to be considered for
future clinical trials run by Triclinium, please click on the
link below and forward your information to us.
Clinical trial sites periodically require the services of trained
Study Nurse/Co-ordinators, usually on fixed-term contracts for
specific trials. Our sites often ask us to recommend suitable
experienced candidates. If you would like to be considered for
future clinical trials run by Triclinium, please click on the
link below and forward your information to us.
Clinical Research Services
