Clinical Quality Associate Director

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Are you ready to make a significant impact in the world of oncology? As the Clinical Quality Associate Director (CQAD), you'll be at the forefront of ensuring quality and compliance within the Oncology Site Management and Monitoring (SMM) function.
Reporting to the overseas Director of Quality Management, you'll guide local teams in applying GCP principles, coordinate country-level quality metrics, and advise on regulatory standards and SOPs.
Collaborate closely with SMM leadership to support compliance training, promote standard processes, and align quality strategies across countries and regions.
Are you up for the challenge? About Astra Zeneca Astra Zeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of diseases in four therapy areas – Oncology; Cardiovascular, Renal and Metabolism (CVRM); Respiratory & Immunology (R&I); and Rare Disease.
At Astra Zeneca Australia, we have been working to deliver the best value to patients for more than 60 years, and we push the boundaries of science to deliver life-changing medicines.
What You'll Do Support the implementation of the Late Development Oncology (LDO) Clinical Operations Quality Framework and serve as the primary contact for quality and compliance across SMM Oncology country teams, ensuring excellence in clinical trial delivery.
Drive country-level quality planning and execution for the Oncology Portfolio in collaboration with other Astra Zeneca compliance-supporting functions.
Ensure adherence to GCP and internal clinical operations standards, maintaining local procedures and guidelines.
Lead all aspects of training compliance, deliver onboarding and ad hoc quality training, and communicate global process updates.
Support resolution of compliance issues and investigations, including CAPA approvals and quality event management in Veeva Quality Vault, while promoting standard process sharing across SMM Oncology teams.
Champion a strong quality culture, contribute to audits and inspections, and serve as SME for SMM quality processes.
Analyse and interpret local quality metrics to drive performance and proactive issue management.
Collaborate with country leadership as a member of the local country SMM leadership team to handle quality reviews, risk registers, and mitigation plans.
Essential For The Role In-depth knowledge and broad experience within the pharmaceutical (biopharma) industry in a Gx P regulated environment.
Understanding of the drug development process and related GXP activities Excellent understanding of the skills and knowledge required for the successful delivery of a clinical study, e.g., ICH-GCP, study management.
Excellent knowledge of international regulations and guidelines.
Excellent interpersonal skills with a proven track record to effectively network cross functionally and globally.
Critical thinking, influencing and strong risk-based decision-making skills.
Ability to collaborate, network and interact widely and effectively at all levels.
Desirable for the role Good analytical, problem solving, negotiation and conflict resolution skills.
Ability to multi-task.
Proven ability to set and handle priorities, performance targets and project initiatives in a global environment.
Ability to collaborate proactively, deal with ambiguity, ability to build strong customer relationships and strategic working partnerships to operate across multiple domains enabling process and system harmonization and standardization.
Why Astra Zeneca? At Astra Zeneca we're dedicated to being a Great Place to Work.
Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit.
There's no better place to make a difference to medicine, patients and society.
An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development.
We're on an exciting journey to pioneer the future of healthcare.
So, what's next Are you already imagining yourself joining our team? Good, because we can't wait to hear from you.
Are you ready to bring new ideas and fresh thinking to the table? Brilliant We have one seat available and we hope it's yours.
Where can I find out more? Follow Astra Zeneca on Linked In: Linked In URL Visit our website: Astra Zeneca in Australia has been formally recognised as an Employer of Choice for Gender Equality by the Workplace Gender Equality Agency (WGEA) and as a Silver Tier Employer within the Australian Workplace Equality Index (AWEI).
Visit our ANZ Careers Page: to learn more about our commitment to fostering a flexible, diverse, and inclusive environment.
We recognise that any recruitment process may present challenges; if there is anything we can do to make our recruitment process more accessible for you, please let us know.
Date Posted 21-Aug-2025 Closing Date 19-Sept-2025 Astra Zeneca embraces diversity and equality of opportunity.
We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.
We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.
We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
Seniority level Mid-Senior level Employment type Full-time Job function Quality Assurance Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Astra Zeneca by 2x Get notified about new Quality Associate jobs in Macquarie Park, New South Wales, Australia.
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