Base: $112,628 (pro rata); bonus/equity: not speci...
Part-time (0.4 fte)
Clinical trial procedures and documentation
Ethics and regulatory compliance
Trial site coordination and monitoring
The University of Sydney is seeking a part-time Clinical Trial Research Support Officer for a 12-month fixed-term role at the Westmead Applied Research Centre. The position involves overseeing clinical trial processes, ensuring compliance with ethical standards, and collaborating with various stakeholders to facilitate successful trial operations
Job Summary
The WARC (Westmead Applied Research Centre) is looking for a proactive Clinical Trial Research Officer to help drive the success of our clinical trials.
In this role, you’ll support trial operations from start-up to closeout, including ethics and regulatory submissions, site coordination, data management, and monitoring.
You’ll collaborate with investigators, research teams, and stakeholders to ensure trials run smoothly, meet milestones, and maintain the highest standards of quality and compliance.
Matching Summary
Match Score: 85
The University of Sydney is seeking a part-time Clinical Trial Research Support Officer for a 12-month fixed-term role at the Westmead Applied Research Centre. The position involves overseeing clinical trial processes, ensuring compliance with ethical standards, and collaborating with various stakeholders to facilitate successful trial operations.
Salary
Base: $112,628 (PRO RATA); Bonus/Equity: Not specified; Benefits: 17% superannuation
Skills & Requirements
Must-have
clinical trial procedures and documentation
ethics and regulatory compliance
trial site coordination and monitoring
data collection and quality management
financial management of trial budgets
collaboration with investigators and stakeholders
Nice-to-have
team leadership and mentoring
change management and continuous improvement
strong problem-solving abilities
high-level computing skills
effective interpersonal communication
promoting safe and inclusive work environment
Key Requirements
knowledge of ICH-GCP guidelines
understanding of ethical and regulatory requirements