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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