Job Title: Clinical Research Coordinator
Clinical Trial Study Support Specialist (0.6 FTE) is a key role in the conduct of clinical trials at a research clinic in Sydney. The successful candidate will support long-term partnerships with pharmaceutical companies, working on innovative studies in Cardiology.
Responsibilities:
1. Provide administrative support to the investigative site.
2. Coordinate study recruitment activities and schedule visits.
3. Transcribe source document data into EDC, including managing query responses.
4. Coordinate study-related tasks and procedures to ensure smooth trial operations.
5. Maintain and archive study documentation.
6. Assist the Principal Investigator with study close-out activities.
7. Support audit processes as needed.
Requirements:
* Degree in Healthcare, Science, or a related field preferred.
* Experience at a clinical research site is essential.
* Knowledge of Cardiology is advantageous.
* Ability to work autonomously and meet expectations.
* Strong communication skills, both verbal and written.
* Proficiency in IT systems, including spreadsheets and data management tools.
What We Offer:
We value our people and strive to build a diverse, high-performing culture. Along with a competitive salary, we offer various benefits focused on well-being and work-life balance, including annual leave entitlements, health insurance options, retirement planning schemes, and more.
Our Commitment:
We are dedicated to inclusion and diversity. We provide a workplace free of discrimination and harassment. If you require accommodations during the application process, please contact us through this link.