Clinical Trials Coordinator X2
Two positions available with USC Clinical Trials Centre - one at Morayfield, one on the Sunshine Coast.
Summary about this job
Research & Fellowships
Company: University of the Sunshine Coast
Location: Sunshine Coast
Work type: Full Time
Salary: n\a
Phone: +61-2-4484-7476
Fax: +61-2-3111-8427
E-mail: n\a
Site: n\a
Detail information about job Clinical Trials Coordinator X2. Terms and conditions vacancy
Morayfield and Sunshine Coast
- Full-time, fixed-term positions, 2 years duration
- Salary: Classification Level 5 (Salary range A$66,509 to A$74,951 gross per annum plus up to 17% employer super)
- One position based at the Morayfield Health Hub and the other position based at the Sunshine Coast.
The University of the Sunshine Coast (USC) has established a world class Clinical Trials Centre, which through partnerships with medical experts and industry is bringing advanced treatments and breakthrough therapies to our communities. The Clinical Trials Centre is seeking two Clinical Trials Coordinators to join their expanding team.
Overview
The Clinical Trials Coordinator (CTC) supports the implementation and conduct of clinical research in accordance with the appropriate quality standards, regulations, rules and guidance. The key focus of this role is to support the coordination and administration of designated clinical trials. The CTC will perform diverse administrative duties requiring analysis, sound judgment, and knowledge of study specific protocols.
Responsibilities
Some of the key responsibilities include:
- You will assist with study start-up, HREC submission, recruitment, screening and enrolment of research subjects, subject adherence to the research protocol, data collection and reporting, study drug/device accountability, monitoring of participants, education of investigators and health care professionals, research subjects and their families and communications with the research team.
- Provide administrative support for designated research projects and programs, including maintaining/using relevant information systems, databases and record-keeping systems
- Assist in the coordination of multiple clinical trials simultaneously ensuring full compliance with local, state and federal policies and procedures.
Requirements
To be considered for this role, you must have the following:
- A tertiary qualification in Health Science/Bio-Medicine or similar education/training and experience.
- Knowledge of ICH Good Clinical Practice and applicable regulations.
- Sound understanding of privacy principals governing health information.
- Previous Clinical Trial Coordination experience highly regarded.
- Nursing qualifications would be beneficial - Registered Nurse applicants must have current registration with AHPRA as a Registered Nurse. Enrolled Nurse applicants must be medication administration endorsed and have phlebotomy training and experience.
- Travel to other sites will be involved.
Apply
All applicants must provide both a statement of claims and resume/curriculum vitae. Obtain the role statement and information regarding how to prepare and submit your application from our website, http://www.usc.edu.au/connect/work-at-usc.
You must have a current right to work in Australia to apply for this job.
Applications close: Midnight Thursday 26 July 2018
More information:
Georgina Street
Clinical Trials Operations Manager
Clinical Trials Centre
07 5456 3798
[email protected]