Do you have extensive study contracts experience and sharp negotiation skills?
Use them to speed up study start-up and accelerate therapy delivery for people living with serious disease.
If you would like to apply your expertise in a company that follows the science and turns ideas into life changing medicines, then AstraZeneca might be the one for you!
About AstraZeneca
AstraZeneca 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 AstraZeneca Australia, we have worked for more than 60 years to deliver the best value to patients.
We advance the frontiers of science to develop life‐changing medicines.
Operating as part of a new, fast‐growing global cell therapy organisation, we are building the frameworks, networks and capabilities needed to accelerate novel, complex therapies to patients.
What You'll Do
The Study Contract Manager at AstraZeneca plays a meaningful role in negotiating and budgeting clinical trials.
You'll develop and manage contracts with investigators, institutions, or external vendors while ensuring integrity, fairness, and regulatory compliance.
Reporting to the regional Study Start Up Director, this role is based in Sydney with hybrid working (in the office 3 days/week).
Key Responsibilities
Lead clinical site contracts and budgets: adapt global agreement templates to local requirements and SOPs, ensuring ethical, fair and compliant practices.




Negotiate with study sites: own budget development using Fair Market Value, and negotiate agreement language and financial terms with investigators and institutions.
Drive timely site start‐up: track and manage agreement status, amendments, payments and issues to enable efficient execution and inclusion in the TMF.
Partner with Legal and stakeholders: act as the point of contact with Legal to safeguard contract integrity; collaborate with study teams and external partners.
Support audit readiness: maintain compliant documentation and contribute to internal and external audits across studies.
Champion improvements: contribute to process enhancements, knowledge sharing, and mentoring of colleagues on financial/contractual practices and support preparation and negotiation of a local Master Service Agreement.
Essential For The Role
Bachelor's degree in life science, law, finance, or equivalent qualification.
Strong knowledge of ICH‐GCP and relevant local regulations; basic GMP/GDP awareness.
Extensive clinical trial contracting expertise (5‐7 years) with demonstrable negotiation skills and FMV‐based budget development within pharmaceutical (preferred) or CRO environments.




Understanding of clinical study management in complex therapeutic areas (e.g., oncology), including monitoring, study drug handling and data management.
Process improvement mindset with strong analytical and problem‐solving skills; ability to manage multiple deadlines.
Meticulous attention to detail with effective written and verbal communication and collaboration skills.
Ability to travel nationally as required.
Desirable
Experience in remote collaboration across dispersed teams and stakeholders.
Post‐graduate training in contracts administration or paralegal experience in pharma/healthcare.
Familiarity with risk‐based monitoring and valuable cultural awareness in international studies.
Tech‐savvy with ability to use e‐enabled systems/software in clinical operations.
Therapeutic area knowledge and ability to learn relevant AstraZeneca therapeutic areas.
AstraZeneca embraces diversity and equality of opportunity.
AstraZeneca 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 believe that the more inclusive we are, the better our work will be.
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.
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📌 Study Contracts Manager - Cell Therapy (Sydney)
🏢 AstraZeneca
📍 Sydney