Medical Evidence Delivery Manager
About the role
About AstraZeneca
About Medical Evidence Delivery
What you’ll do
As a Medical Evidence Delivery Manager, you will drive the operational delivery and governance of Medical Affairs evidence-generation activities across Australia and New Zealand. You will focus mainly on externally funded studies, such as investigator-initiated research, and emerging real-world evidence initiatives. You will collaborate with investigators, Medical leaders, and global partners to bring approved research programmes to life
- Act as the primary operational contact for ESR activities, from proposal review through contracting, study maintenance and AstraZeneca close-out.
- Collaborate closely with investigators, Medical teams, and global colleagues to coordinate reviews, approvals, governance activities, documentation and study achievements.
- Bring an operational and feasibility perspective to evidence planning, partnering with Medical and evidence owners to translate scientific priorities into deliverable research activities.
- Coordinate research agreements, fair market value, financial support and related processes with functional owners, maintaining accurate, audit-ready records and systems.
- Track timelines, budgets, vendors, risks, dependencies and contractual deliverables, proactively identifying issues and coordinating appropriate responses with the team.
- Support publication review, study close-out, operational metrics, continuous improvement and agreed cross-cover for defined Medical Affairs study-delivery activities.
- Contribute to continuous improvement of evidence-delivery processes, tools and ways of working across Medical Affairs.
Essential to the position
- Tertiary qualification in life sciences, pharmacy, public health, health sciences, clinical research or another relevant field, or equivalent relevant industry experience.
- Demonstrated experience coordinating or managing clinical research, ESR, evidence-generation studies or comparable regulated projects.
- Proven project-management capability across multiple collaborators, achievements, risks and deliverables.
- Working understanding of research governance, documentation, contracting, financial and compliance requirements.
- Proven ability to build effective relationships with investigators, research partners and cross-functional collaborators.
- Ability to work effectively across functions and influence team members without direct authority.
- Strong organisational skills, attention to detail, judgement and practical problem-solving capability.
Desirable for the role
- Experience in pharmaceutical, biotechnology, contract research, academic research or healthcare environments.
- Experience with Externally Sponsored Research (ESR) including investigator-initiated or investigator sponsored studies/research (IIT/IIS/ISR/IIR), Phase IV studies, non-interventional studies, real-world evidence, registries or secondary-data research.
- Experience with research agreements, study budgets, vendor management, study documentation, publication processes or evidence-management systems.
- Working knowledge of Australian and New Zealand research governance, privacy, safety and applicable industry requirements, including ICH-GCP where relevant.
- Experience supporting study disclosure, audit/inspection readiness or continuous improvement in a regulated environment.
Why AstraZeneca?
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.
Guidance on AI use
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Where can I find out more?
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Date Posted
Closing Date
Not included in the source posting: qualifications, benefits.
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