
Clinical Research Associate
3 days ago
This role will provide a challenging and rewarding career path that supports growth and professional development, broadening expertise in trial monitoring.
As a Clinical Research Associate, you will have the opportunity to work on first-in-class Oncology trials, developing high-quality medicines for the treatment of cancer and other major diseases. You will be involved in the full lifecycle of a trial, from site identification and start-up through to close-out.
Key Responsibilities- Perform generalist CRA duties, including site selection, site activation, site initiation, routine monitoring visits, close-out visits, and database lock.
- Lead site identification and initiation activities in Australia, including HREC/RGO process.
- Oversee all aspects of study site management to ensure high-quality data and consistently low query levels.
- Degree in Pharmacy or related field.
- At least 3.5 years of prior monitoring experience with global trials, including strong Oncology monitoring experience.
- Working experience with initial Australian ethics and regulatory submissions.
- Excellent communication skills, adaptability, and ability to work autonomously.
- Good knowledge of international guidelines ICH-GCP and local regulations.
- Flexibility to travel for monitoring visits as required.
This role offers a unique opportunity to contribute to the development of life-changing treatments and work with a talented team of professionals.
Further InformationThe successful candidate will be based in Australia. The company is an equal opportunities employer and welcomes applications from diverse candidates.
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