The Clinical Trials Coordinator undertakes the administration of the clinical research conducted by the Department of Haematology/Oncology, in accordance with Good Clinical Research Practice (GCRP), NHMRC guidelines and standard operational procedures (SOPs) in conjunction with the Investigator and the Clinical Trials Manager.

 

The Clinical Trials Coordinator coordinates the screening procedures for study entry and subsequent randomisation/registration to the study.  Duties include but are not limited to, the discussion of study logistics with participants, the coordination of participant appointments and clinical follow-up ensuring protocol compliance, the close monitoring of participants while on study, the collection of source data and test results and the input of data into participant case report forms, the collation and processing of specimens and the immediate reporting of serious adverse events.

 

In addition to the above, the Clinical Trials Coordinator is involved in managing the documentation and compilation of clinical research data, and providing operational support for the delivery of clinical trial submissions, reporting, and other approval requests that are required by Lead Ethics Committee or Research Governance.

 

Bachelor degree covering fields relevant to role in the research program or project.

 

The South Australian public sector promotes diversity and flexible ways of working including part-time. Applicants are encouraged to discuss the flexible working arrangements for this role. 

Appointment will be subject to a satisfactory Criminal History Check and compliant Immunisation screening. 

Aboriginal and Torres Strait Islander applicants are encouraged to apply.

 735022 Clinical Trials Coordinator1.pdf