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About Clinical Research at AstraZeneca
AstraZeneca's vision in Oncology Research & Development (R&D) is to push the boundaries of science to change the practice of medicine, transform the lives of patients living with cancer, and ultimately eliminate cancer as a cause of death. Our broad pipeline of next-generation oncology medicines has nearly 100 clinical trials ongoing. The Site Management and Monitoring (SMM) organization is responsible for delivering cost-effective and high-quality study data to Oncology R&D. We work across approximately 40 countries, managing and monitoring activities focused on protecting patients, supporting investigators, and ensuring reliable data is delivered. Our scope includes phase I-IV studies at global, local, and regional levels. We focus on internally-led studies supporting various Therapeutic Areas including lung, breast, gastrointestinal, genitourinary, and hematology.
About the Programme
Our program provides a springboard to your future career as a Clinical Research Associate (CRA). Our Graduate Programme offers opportunities throughout the 1-year program to make real contributions and work on projects supporting teams in three placements including Trial Master File Administration, Study Start-Up, and Site Monitoring. Supported by experts in their field, you will receive mentoring and training to expand your knowledge and prepare you for a career as an Oncology CRA.
What you can expect
What you will be doing
Our program is designed to help you understand the way we work support the overall delivery of the oncology portfolio and provide insights into the collaborative, cross-functional CRA role. Through the placements, you will develop skills in building and maintaining multi-disciplinary relationships. Over the course of the program, you will receive mentoring and feedback from managers and colleagues, so you'll be able to identify areas of strength, as well as those you want to further develop.
Placement 1: Trial Master File Administration
You will learn and become an expert on the essential documents required to support a site's electronic Trial Master File (eTMF). You will collect, quality-check and file regulatory documents from oncology institutions that support the delivery of the study.
Placement 2: Study Start-Up
You will join the internal Study Start-Up (SSU) team, working to quickly and efficiently support a site through to activation.
Placement 3: Site Monitoring
You will be undergoing a series of trainings including oncology-focused modules and mock visit opportunities, all to learn how to be a successful oncology monitor. There will also be opportunities to attend and observe a monitoring visit with an experienced oncology monitor.
Post-Programme:
Upon completion of the program, there is an opportunity for a full-time CRA position based on participant interest, performance, and business needs.
To be eligible for the program, you'll need:
Application Period: 9 April to 3 May 2026.
Interview Period: 13 May to 15 May 2026
On-Boarding Period: 1 June 2026
Why AstraZeneca
At AstraZeneca, 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 in medicine, patients, and society. An inclusive culture that champions diversity and collaboration, and is always committed to lifelong learning, growth, and development. We're on an exciting journey to pioneer the future of healthcare.
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Job ID: 146591641