Employment OS for your Business

Start Up Specialist (Clinical Research)

Parkville, Victoria 3052, Australia • Full-time
AI Job Summary
  • At least 12 months’ experience in a medical or related administrative role.
  • Experience coordinating and/or reviewing human research ethics applications for clinical trials.
  • Ensure compliance with ethics and governance components and ICH-GCP guidelines and requirements.

Role Type

Permanent • Full-time • Associate

Description

Start Up Specialist (Clinical Research)

  • Full-time, permanent position – Part-time, 0.8FTE will also be considered.
  • Friendly and supportive culture.
  • Flexible working arrangements.
  • $74,000-$80,000 Base Salary + NFP salary packaging benefits.

Join a supportive Ethics and Governance team to build the foundations to a fulfilling and rewarding clinical research career!

About Us

Cancer Trials Australia (CTA) is a not-for-profit member-based organisation consisting of 33 clinical sites and 3 medical research institutes across Australia and New Zealand. We support the administration and management of clinical trials across both metropolitan and regional hospitals. We work in close partnership with clinical research sites, Sponsors and Contract Research Organisations to ensure patients can gain access to appropriate clinical trials as quickly as possible. CTA is committed to developing internal talent and places great emphasis on nurturing a culture of compassion and purpose in the workplace.

CTA is committed to equal employment opportunity and ethical practices. We recognise the rich diversity of people and the value that brings to the workplace. We support a culture of equity, inclusion, and diversity. This position is open to all people. 

Employee Benefits

  • Additional Leave Entitlements – 5 weeks annual leave and 14 days personal/carer’s leave.
  • Salary packaging available of up to $15,900 + $2,650 meals/entertainment to maximise your take home pay.
  • A flexible and hybrid working environment.
  • Access to a robust Learning Management System, including support towards a personal learning and development budget.
  • Access to an Employee Assistance Program (EAP).
  • Company paid parental leave.

About the Role

As part of the Operations team, you will be part of a collaborative and supportive team that is responsible for providing high levels of administrative and customer service support. This role will coordinate ethics and governance submissions of clinical trials to ensure their effective and timely approval and implementation.

Our Ethics Submission Specialists, as this role is known internally, liaise closely with Research teams (Study Coordinators, Principal Investigators, and Research Unit Managers) at Clinical Research Sites, as well as staff from Human Research Ethics Committees and Research Governance Offices. You will also nurture strong relationships with local and global CRO’s, as well as national and international biotechnology and pharmaceutical companies.

In this role you will:

  • Demonstrate your project management skills by prioritising tasks and balance competing deadlines.
  • Be responsible for conveying and interpreting complex medical information to a range of different audiences.
  • Ensure compliance with ethics and governance related components, to meet local ICH-GCP guidelines, requirements of human research/ethics offices and sponsoring companies.
  • Lead the review and management of detailed documents containing scientific information and carefully monitor the status and progression of concurrent submissions.

About You

The ideal candidate will have excellent administration and communication skills with a strong focus on customer service. You will be a team player, who thrives in delivering quality outcomes to clients.

Qualifications and experience:

  • At least 12 months’ experience in a medical or related administrative role.
  • Demonstrated experience in the coordination and/or review of Human research ethics applications would be highly advantageous (preferred but not essential).
  • Tertiary qualification in Health, Life Sciences, or other related qualifications, with a sound working knowledge of medical terminology/scientific language (preferred but not essential).
  • Excellent attention to detail.
  • Highly developed organisational and time management skills.

Candidates located beyond our Melbourne office-based region are encouraged to apply, as fully remote arrangements may be considered for this role.

To view the position description for this role, please copy and paste the link provided below into your web browser:

https://cancertrialsaustralia.com/wp-content/uploads/2026/01/Ethics-Submission-Specialist_PD-2025.pdf

For any further queries about this opportunity email: employment@ctaust.org

Please note, the successful applicant will be required to supply a current National Police Check.  

Closing date for applications: Wednesday, 27 May 2026 at 5pm 

Only shortlisted candidates will be contacted within a week of the closing date.  

 

Shared Purpose | Integrity | Collaboration | Adaptability | Compassion

Company Overview

Purposeful not-for-profit organisation that supports the management of a large number of oncology clinical trials in an effort to advance novel therapeutics to improve the outcomes for people affected by cancer.