
Principal Research Professional
2 days ago
This is an exciting opportunity to work as a Clinical Research Associate in a globally recognized clinical research organization. You will have the chance to make a positive impact on human health and develop your career in a values-driven environment.
The Clinical Research Associate will play a vital role in the management and monitoring of clinical trial sites, ensuring the smooth operation of clinical studies from initiation through to close-out.
Key Responsibilities- Site Management & Monitoring
- Study Progress & Documentation
- Site Feasibility & Investigator Recruitment
- Safety Reporting
To be successful in this role, you will need a minimum degree qualification and at least 2-3 years of independent on-site monitoring and site management experience.
You will require extensive knowledge of ICH-GCP guidelines and SAE reporting, as well as strong verbal and written communication skills, and the ability to work effectively within a project team and matrix environment.
Why Work with Us?- Join a highly regarded CRO with a strong family culture
- Work on globally recognized clinical research studies
- Enjoy four wellness days off a year (in addition to four weeks' leave) and a birthday day off
- Relish flexible working options and free parking in our Hawthorn East location
- Pursue career development opportunities within our organization
- Benefit from a referral bonus for introducing great candidates
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