Clinical Research Associate

Clinical Research Associate

Work Type:

Full Time

Location:

Sydney - NSW 

Industry:

Clinical Research

Contact Name:

Angela Barclay

Contact Email:

abarclay@onqrecruitment.com.au

Contact Phone:

0415508607

Date Published:

09-Jul-2025

Expiry Date:

Clinical Research Associate
In partnership with the Australasian Gastro-Intestinal Trials Group (AGITG)
Location: Sydney| Full-Time | Permanent

Make a meaningful impact on health outcomes through innovative clinical trials.
Are you passionate about clinical research and ready to contribute to cutting-edge, investigator-led trials? Join a dedicated team at the AGITG within their Clinical Research Centre (CRC) as a Clinical Research Associate (CRA). This is a fantastic opportunity to play a key role in improving healthcare while developing your career in a collaborative and purpose-driven environment.

About the Role
As a CRA, you’ll be at the forefront of trial delivery—supporting the full trial lifecycle from setup to close-out across multiple clinical sites. You’ll collaborate with internal team members, site investigators, vendors, and clinical site staff to ensure high-quality, ethical trial conduct aligned with Good Clinical Practice (GCP) and regulatory requirements.
This role involves a mix of on-site and remote monitoring and requires domestic travel.

Key Responsibilities

  • Conduct site feasibility, start-up, initiation, monitoring, and close-out visits
  • Ensure data quality through source data verification and adherence to protocol
  • Support ethics and regulatory submissions, including TGA applications
  • Maintain the Trial Master File and essential study documents
  • Provide guidance and training to site teams and monitor site performance
  • Work collaboratively with study chairs, investigators, and CRC team members
  • Contribute to trial planning, documentation, and reporting
  • Lead issue resolution and ensure participant safety and compliance
About You
You’re a proactive and detail-oriented clinical research professional with:
  • A degree in a relevant discipline (e.g., life sciences, health, clinical research)
  • Solid experience in clinical trial monitoring within academia, CRO, or pharma where Oncology experience would be highly desirable
  • In-depth knowledge of ICH GCP and Australian regulatory frameworks
  • Strong communication skills and a collaborative mindset
  • The ability to manage competing priorities while maintaining high accuracy
  • A valid Australian driver’s licence and willingness to travel domestically
Desirable
  • Experience in oncology clinical trials
  • Strategic thinking and a solutions-focused approach
  • Confidence in managing trial documentation and site communications
Why Join AGITG?
At AGITG you’ll be part of a supportive, multidisciplinary team committed to advancing health through innovative research. You’ll have the chance to work on high-impact studies and build strong relationships across the research network while contributing to national and international trial success.

Ready to make a difference in clinical research?
Apply now and join a team where your work truly matters.

APPLY NOW
Interested in this job?
Save Job

Share this Job

Create Alert

Similar Jobs

Read More
Return to Job Search
SCHEMA MARKUP ( This text will only show on the editor. )