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Clinical research associate

Brisbane
Accelagen Pty Ltd
Clinical Research Associate
Posted: 14 September
Offer description

Clinical Research Associate - II, III or Senior
Clinical Research Associate - II, III or Senior
This range is provided by Accelagen Pty Ltd. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
A$80,000.00/yr - A$130,000.00/yr
Direct message the job poster from Accelagen Pty Ltd
Join this rapidly growing global Clinical Research Organisationfor a chance to have a positive impact on human health around the world.
· Grow your career in this values driven CRO
· HO in Hawthorn East, offering hybrid working and free onsite parking for those in Melbourne
· A fun, family culture & dynamic environment offering meaningful work
About our business
We are a leading, locally positioned and globally adept Clinical Research Organisation (CRO) headquartered in the Melbourne suburb of Hawthorn East. We are working with innovative clients across the globe to make a tangible impact on the future of human health and wellness.
Celebrating 15 years in 2025, our experience is widely varied across the health, wellness and disease spectrum. We offer end-to-end services across Strategic Consultants, Clinical Trials, Regulatory Affairs & Biometrics.
We are experiencing rapid growth and currently have an opportunity for an experienced Clinical Research Associate II, III or Senior level to join our team.
As a CRA, you will play a crucial role in the management and monitoring of clinical trial sites, ensuring the smooth operation of clinical studies from start-up through to close-out. You will work across a variety of protocols, sites, and therapeutic areas, ensuring the integrity and quality of clinical research data.
Key Responsibilities
Site Management & Monitoring
Study Progress & Documentation
Site Feasibility & Investigator Recruitment
Safety Reporting
The ideal, minimum Degree qualified candidate will have the following:
Minimum of at least 2-3 years of independent on-site monitoring and site management experience.
Extensive knowledge of ICH-GCP guidelines and SAE reporting.
Ability to work effectively within a project team and a matrix environment.
Detail-oriented with a solid understanding of clinical trial procedures and regulatory guidelines.
Strong verbal and written communication skills & the ability to work independently, self-manage, and proactively identify and resolve issues.
Strong problem-solving skills and ability to manage complex issues.
Must be willing to travel interstate for study site visits.
Valid Driver's License is required.
This position can be located anywhere in Australia - Ideally QLD in the short term. We are unable to accept applicants who do not have Australian Work Rights at this time.
Why work for Accelagen?
· An opportunity to change the world working for a highly regarded CRO with strong family values
· Working on globally recognised Clinical Research studies
· 4 Wellness days off a year (in addition to 4 weeks leave) & a day off for your Birthday
· Hawthorn East location, with free parking and hybrid/ flexible working
· Career development opportunities within the organisation
· Referral bonus – know someone great...get rewarded for the intro
Seniority level
Seniority level
Not Applicable
Employment type
Employment type
Full-time
Job function
Job function
Research
Industries
Research Services and Biotechnology Research
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