Clinical Trials Assistant

Job No: GEORGE194
Location: Newtown, Sydney

  • Full time (1 FTE)
  • Fixed term contract (1 year)
  • Respected global research organisation
  • Make an impact on global health outcomes

The George Institute is 700 people around the world, all focused on improving the health of millions of people worldwide. As a medical research institute affiliated with leading universities and with projects in approximately 50 countries, we are challenging the status quo in healthcare to:

  • Find better treatments for the world's biggest health problems
  • Transform primary health care to support better health for more people
  • Harness the power of communities, governments and markets to improve health

Our innovative commercial enterprises help maximise our impact. Please visit 'what we do' to read more about how we are addressing the world's biggest health problems.

We have a new and exciting opportunity for a Clinical Trials Assistant to join our growing organisation. The Clinical Trials Assistant (CTA) is required to assist the Project Managers and study teams with various tasks associated with running a large-scale clinical trial and other clinical research projects within the division. The role requires the individual to provide administrative and project tracking support during the development, execution and closure of clinical research projects.

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
  • Responsible for the maintenance and filing of study administrative files
  • 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
  • Provide other administrative support to study team and division

Success will be based on a range of key skills and experience, including but not limited to:

  • Tertiary qualification in a health or science discipline
  • Some understanding of medical terminology
  • Relevant experience in a clinical research environment
  • Basic knowledge of clinical trial processes and ICH/GCP guidelines desirable
  • Strong general administration skills and experience
  • High proficiency in the use of the Microsoft Office suite of products, including Word, Excel, PowerPoint, Publisher and Outlook and the Internet
  • Excellent interpersonal skills and the ability to work well and flexibly i.e. autonomously, in small teams and with a wide range of varying stakeholders
  • Ability to see the big picture, yet still focus on detail
  • Ability to be flexible and adaptable in the face of changing organisational priorities and ambiguous environments
  • Strong focus on quality of work

This is a great opportunity for you to work on exciting projects and make an impact on global health outcomes. To learn more about the role, please view the Position Description here.

The closing date for applications is Thursday 3rd September 2020. We do, however, reserve the right to close this vacancy early if a suitable candidate is found.

Please apply now!

 

Our big and bold mission to improve the health of millions of people worldwide needs a diverse and innovative team to deliver it. So we foster a dynamic, inclusive and flexible workplace where each individual can bring their best selves to work.

Everyone is encouraged to apply, including people with a disability; women; Aboriginal and Torres Strait Islander people; people who identify as LGBTIQ; mature-aged adults and those from culturally and linguistically diverse backgrounds.

Apply Now

Privacy Acknowledgment

The George Institute for Global Health, together with its subsidiaries and associated companies worldwide (“The George Institute”, “we” and “our”) is committed to handling personal information (including health and other sensitive information) in accordance with applicable privacy laws, including the Australian Privacy Principles (“APPs”) set out in the Australian Privacy Act 1988 (Cth).

When you apply for a job at the Institute you will be asked to set up an account and apply for any of the jobs posted in the system. You may be asked to submit personal information including, but not limited to: a) your name; b) your address; c) your email address; d) your telephone number; e) and other personal and sensitive information.

Any personal information you submit to our recruitment system will be used to process your application and is retained in the database to match your skills against any future job opportunities. We may contact you about your current job application/s and any future job opportunities that match your criteria.

The George Institute works with people from diverse cultural and social backgrounds with varied life experiences, physical abilities and interests and we seek to employ people who reflect the great diversity of people. We may ask personal questions regarding your identity, which will be used to inform our Diversity, Inclusion and Belonging strategies with regards to recruitment. You may elect to not disclose this information.

I consent to The George Institute of Global Health to collect, use and disclose my personal information for the purpose of assessing and facilitating my application for employment.

Please see following link for more information on how the George Institute may collect and use your data: https://www.georgeinstitute.org/privacy-policy


Personal Details * Required field

Questions

Why work at the George?

We are committed to attracting, developing, rewarding and retaining the best people in their fields to conduct and support our innovative and highest quality research programs.