Clinical Study Administrator (CSA) Graduate Program
About The Position
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. 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.
Requirements
- 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%.
Nice To Haves
- 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.
Benefits
- qualified retirement programs
- paid time off (i.e., vacation, holiday, and leaves)
- health, dental, and vision coverage
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
