AstraZeneca
Location
Wilmington, Delaware
Salary
$85,000 / YEAR
Participants in the CSA Graduate Program will work on clinical trials for oncology medicines, contributing to the collection and filing of regulatory documents and study site activation. The program includes rotations through various teams to understand their roles in delivering the oncology portfolio.
Candidates must have a bachelor's degree in a relevant field awarded in 2025 or 2026 and demonstrate the ability to manage multiple priorities in a fast-paced environment. Up to 2 years of prior work experience, including internships, is desired, along with an understanding of clinical trial processes.
Wilmington, DE (On-site) Be at the heart of bringing life-changing medicines to the world. As part of our Clinical Study Administrator (CSA) Graduate Program, you’ll work on clinical trials for our innovative portfolio of oncology medicines, directly influencing our ability to provide treatments and impact the lives of millions of people globally.
AstraZeneca’s vision in Oncology Research & Development (R&D) is to push the boundaries of science to change the practice of medicine and to 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 delivers high-quality study data to Oncology R&D. We work across approximately 40 countries, monitoring activities of phase I-IV trials across Therapeutic Areas including lung, breast, gastrointestinal, genitourinary, and hematology About the Program Our program provides a springboard to your future career as a CRA. Starting in September 2026, you will progress through three five-month rotations within the SMM organization, supporting teams in Trial Master File Administration (eTMF), Study Start-Up, and Site Monitoring. The rotational assignments are designed to help you understand how each team supports the overall delivery of our oncology portfolio and provide insights into the collaborative, cross-functional CRA role. You will make real contributions and work on projects supporting collection and filing of regulatory documents and study site activation. Participants receive training, including oncology-focused modules, engage in mock visits, and observe monitoring visits with experienced oncology monitors. Through the placements, you will develop skills in building and maintaining multi-disciplinary relationships. You will receive mentoring and feedback from mangers and colleagues, so you’ll be able to identify areas of strength, as well as those you want to further develop. Upon completion of the program, there is opportunity for a full-time CRA position based on participant interest, performance, and business needs. Minimum Requirements for the role: Bachelor’s degree awarded in 2025 or due to be awarded in 2026 in life science, health science, or related field 0 years of experience Demonstrated ability to manage multiple priorities and meet deadlines in a fast-paced environment. Proven experience in planning, organizing, and tracking tasks to ensure timely completion of deliverables. Ability to travel throughout the US up to 50%. Desired for the role: Up to 2 years of prior work experience, including previous internships/co-ops. Understanding clinical trial processes and common regulatory documents, such as data collection, regulatory compliance, or patient interaction. About AstraZeneca in Wilmington, DE Our Wilmington campus is where several business functions integral to our US business are based and where 1,500 of our colleagues innovate for a higher purpose. Conveniently located near Philadelphia, our newly redesigned campus offers a positive and inclusive environment and plenty of on-site perks for employees, including Fitness and Wellness Centers, meditation rooms, walk rooms, and more! Why AstraZeneca? With emphasis placed on personal and professional development, we truly invest in you, your interests, and your potential. Working in a highly fast-paced yet deeply supportive environment, you’ll be encouraged to jump in so you can put your knowledge into practice, but with all the guidance and support you need. So, what is next?
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