Clinical Trials Quality Assurance Specialist

2 weeks ago


Sydney, New South Wales, Australia beBeeCompliance Full time $109,857 - $129,624
Job Title: Quality Manager

This role is responsible for ensuring the quality and regulatory compliance of clinical trials.

Key Responsibilities:

  • Lead and manage clinical trial monitoring and site operations
  • Oversee site readiness for audits and inspections, including risk assessments and mitigation strategies
  • Manage all aspects of site research activities, including trial timelines, data quality, investigational product handling, and staff training
  • Drive operational excellence by developing policies, reviewing incidents, supporting accreditation, and advising on study budgets and processes

Requirements:

  • Relevant tertiary qualifications in life sciences, allied health, clinical research, or business/health administration
  • Minimum 3–5 years' experience in clinical research, including demonstrated ability to work independently and collaboratively, and contribute to quality improvement initiatives
  • Strong leadership, negotiation, and interpersonal skills with the ability to communicate effectively, motivate teams, and manage complex stakeholder relationships
  • Proven ability to deliver accurate, timely reporting and apply robust analytical and financial management skills within a clinical trial or research setting

Benefits:

  • Join an organization that prioritizes quality and regulatory compliance
  • Develop your leadership and project management skills
  • Contribute to high-quality clinical trials and make a positive impact on patient outcomes

About You:

  • We welcome applications from individuals with a strong passion for quality and regulatory compliance
  • If you have a background in clinical research and are looking for a new challenge, we encourage you to apply


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