-
Full time, fixed term for 12 months
-
Renal and Metabolic Division
Key responsibilities of the role will include:
-
Assisting in the preparation of research grant applications, study documentation, study forms and the development of administrative systems and processes
-
Assisting in the distribution of study documents to investigators, site staff and the International Coordinating Centre
-
Tracking study progress including patient screening and recruitment, protocol deviations and data management
-
Assisting in pharmacovigilance activities
-
Assisting Investigational Product and trial supplies management
-
Coordinating the receipt, tracking, labelling and reporting of study blood samples for central analysis
-
Tracking and processing invoices and authorised clinical trial payments
-
Organising and scheduling internal and external meetings.
Desired Skills and Experience
Our ideal candidate will possess:
-
A Bachelor’s degree in a health or science discipline
-
Relevant experience in a clinical research environment
-
Strong general administration skills and experience
-
An understanding of medical terminology
-
Basic knowledge of clinical trial processes and ICH/GCP guidelines desirable
-
Proven proficiency in the use of the Microsoft Office suite of products
-
Excellent interpersonal skills and the ability to work well and flexibly
-
Ability to see the big picture, yet still focus on detail.
Please find further information, position description and application form on our careers page via the link:
http://thegeorgeinstitute.recruitmenthub.com.au/Vacancies/3233192/title/Project-Assistant
