- Remuneration and benefits packages including 17% superannuation contributions; Christmas to New Year leave in addition to annual leave; salary sacrificing options for cars, parking, childcare and more
About the Role
You will be responsible for the development, implementation, coordination, management, and monitoring of clinical trials within CHOIR. You will use your experience in research to devise, implement, monitor, and report on the conduct of research projects from inception, and provide guidance on operational matters. You will also provide input into the development of suitable research networks to support conduct of trials in haematological malignancies, including site selection and ongoing evaluation.
Responsibilities include, but are not limited to:
- Participation in assessment, start-up, and close-out of clinical trial sites
- Operational input during development of clinical trials
- Preparation and management of documentation and materials required for trial conduct
- Preparation and management of ethics and regulatory applications
- Lead relevant project specific meetings and oversee project administration
- Provide guidance and oversight regarding operational conduct of clinical trials and their academic aspects
- Provide timely and focused reports to all stakeholders regarding trial implementation and progress
- Oversee the production of clinical study reports, in collaboration with data managers and study statisticians, and assist academic staff in the preparation of abstracts and manuscripts for scientific meetings and for publication
- Onsite and remote study site monitoring, including report management
- Management of serious adverse event reports and safety information
- Budget and site contract development, general management of trial finances
- Manage relationships with key stakeholders, including representatives from trial sites, industry, academic, and clinical partners
- Ensure all trials are managed and monitored according to the National Statement on Ethical Conduct in Human Research and ICH-GCP requirements
- Participate in team meetings and special projects to develop and improve processes and systems
About You
Our ideal candidate will be a highly motivated and experienced individual who has a strong interest in health research, and who is keen to play a key role in delivering high quality clinical trials.
To be successful in the role, it is essential that you demonstrate:
- Postgraduate qualifications in a public health or biomedical discipline, or progress towards postgraduate qualifications and extensive relevant experience in the conduct of medical research (
- Proven experience planning and coordinating multi-centre clinical trials including monitoring, central laboratory specimen collection, shipment and storage, drug distribution and accountability processes.
- Experience in the development of analysis plans and clinical trials analysis as well as preparation of publications, reports and conference presentations
- Proven ability to work effectively both independently and as part of a multidisciplinary team, including clinical and laboratory stakeholders
- Excellent computer skills including experience and competence in using data collection instruments and programs
- Excellent organisational skills and ability to prioritise own workload and work independently as well as effective member of a team
- High level understanding of equal opportunity principles and a commitment to the application of EO policies in a university context
For further information, please contact Sarah Davidson:
ANU values diversity and inclusion and is committed to providing equal employment opportunities to those of all backgrounds and identities. For more information about staff equity at ANU, visit
Application information
In order to apply for this role please make sure that you upload the following documents:
- A statement addressing the selection criteria.
- A current curriculum vitae (CV) which includes the names and contact details of at least three referees (preferably including a current or previous supervisor). If your CV does not include referees you can complete these online when prompted in the application form.
- Other documents, if required.
Please note: The successful candidate must have rights to live and work in this country and will be required to undergo a background check during the recruitment process. An offer of employment is conditional on satisfactory results.
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