Job Overview
The primary function of the role is to ensure that clinical trials are conducted in accordance with regulatory requirements and guidelines.
Key responsibilities include building relationships with site trial personnel, managing trial data, and ensuring participant wellbeing.
Responsibilities
* Develop strong working relationships with Principal Investigators and other site trial personnel to facilitate smooth trial management.
* Manage trial data accurately and efficiently to meet project timelines and requirements.
* Ensure participant wellbeing by adhering to ICH GCP guidelines and local regulations.
Qualifications & Experience
Applicants must possess a graduate degree in a clinical or life sciences-related field. Relevant experience and qualifications in allied professions may also be considered.
* CRA II: Minimum 6 months independent monitoring experience required.
* CRA III: 2+ years independent monitoring experience required.
* SCRA: Min 4 years CRA monitoring experience required.
Full unrestricted working rights in Australia are mandatory for this role. Sponsorship cannot be provided.
Benefits
We offer flexible working arrangements and full flexibility in working hours to ensure staff achieve work-life balance.
Other benefits include paid parental leave, flexible leave entitlements, wellness programs, and ongoing development opportunities.
Our company values diversity and inclusion and welcomes applications from people with disabilities, LGBTIQ+ individuals, and those with caring responsibilities.