Clinical Research Associate
1 week ago
This role is ideal for a detail-orientated and proactive individual to support our expanding clinical trial portfolio. As a Clinical Research Associate - Trial Management Specialist, you will be responsible for managing study start-up, monitoring and close out activities.
Key Responsibilities- Coordinate study operations with investigators and institutions.
- Maintain GCP compliance and ensure accurate documentation of study master files.
- Foster strong relationships with clinical trial teams and stakeholders.
- Bachelor's degree in Science, Medical, Healthcare or related field.
- Minimum 1 year experience in pharmaceutical, biotechnology, CRO, and/or academic setting.
- Strong knowledge of clinical trial regulations and GCP guidelines.
- Oncology experience is highly desirable.
- Full working rights in Australia.
This role offers the opportunity to work in a dynamic environment with a growing company. You will have the chance to develop your skills and expertise in clinical trial management.
OthersThe successful candidate will be a team player who is able to work independently and collaboratively as part of a global team. If you are motivated and enthusiastic about clinical research, we encourage you to apply.
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