Clinical Research Assistant

3 weeks ago


Townsville, Queensland, Australia Icon Group Full time
Clinical Research Assistant - Research at Icon Group, Wesley

Research Brisbane Contract or Temp Research at Icon Group

Key Points

- 12-month contract, full-time role based in our site at Icon Cancer Centre Wesley
- All-round Oncology research role
- Join Australia's largest private cancer clinical trials program with access to cutting-edge technology and innovative care solutions.

The Opportunity

Support our research operations and clinical trials undertaken on-site at the Icon Cancer Centre Wesley, contributing to our nationwide trial programs through Icon Research.

- Diverse Oncology Research Experience: Gain hands-on exposure to cancer treatment research, backed by comprehensive support and training from on-site coordinators, team leads, governance officers, oncologists, pharmacists, oncology nurses, and the wider Icon Research community.
- Career Growth & Development: Kick-start your research career with Australia's largest private Cancer Clinical Trials program. Joining us opens the door to unparalleled opportunities for career growth and development within the Icon Group.

About The Role

As a Clinical Research Assistant, you'll support the coordination and administration of Oncology and Haematology Clinical Trials.

Key Responsibilities

- Collect, process and dispatch samples and other materials required by clinical research protocols and prepare and manage clinical trial laboratory kits and samples.
- Prepare patient visit requirements, assist in appointment scheduling and external hospital liaison for tissue requirements or medical information.
- Provide support to the research staff in relation to clinical trial administration tasks.
- Provide support to the investigators conducting clinical trials by ensuring trial documentation is prepared and ready for their review/sign off.
- Manage investigator site files and essential documents as per GCP.
- Facilitate the attributable, legible, contemporaneous, original and accurate collection of source data.
- Work closely with monitors for ongoing monitoring at site and facilitate remote visits.
- Occasionally travel between our clinics as needed to support the conduct and oversight of cross-clinic research activity.

About You

We're looking for someone passionate about Clinical Research with a keen interest in the field of Oncology & Clinical Trials.

Essential Requirements

- Relevant undergraduate degree (or working towards one) in Health Sciences, Nursing or Allied Health.
- Excellent written, verbal and interpersonal skills.
- Proficient in MS office suite and database management.
- Australian working rights and the ability to commit to full-time employment for the duration of the contract.

Desirable

- Experience in Pathology and Laboratory processing.

To Apply

Please attach a resume and cover letter showing us why you'd love to join us, and what makes you a great fit for the role. Icon Group celebrates diversity and is committed to creating an inclusive workplace for all employees. We encourage applications from all diverse backgrounds.

Pre-Employment Health Requirement

Icon is committed to managing the risk of transmission of specified vaccine preventable diseases (VPDs). Certain roles may require the successful candidate to show evidence that they have been vaccinated against or are not susceptible to specified VPDs.

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