Grad Intern - Global Patient Safety (Summer 2027)
About The Position
The Grad Intern will work with the Late-Stage Oncology Clinical Science team to support the execution of oncology clinical trials. The internship provides hands-on experience in clinical data review, study conduct, and cross-functional collaboration, contributing to work that supports development of therapies for patients with cancer. The intern will learn about the clinical scientist role in oncology clinical development through meetings, mentorship, and guided projects. The position is a full-time summer 2027 internship. Interns must remain enrolled at an accredited college or university after the program and be located in the United States for its duration. Applicants must be authorized to work in the United States for the duration of the program; sponsorship for future full-time roles is not guaranteed.
Requirements
- Must be at least 18 years old.
- Must have graduated with a bachelor’s degree from an accredited college or university.
- Must be currently enrolled in an accredited MBA, Master’s, PharmD, or Ph.D. program and complete the first year of that program before the internship starts.
- Must be available to work a full-time schedule.
- Must continue enrollment at an accredited college or university following the internship program.
- Must be located in the United States for the duration of the internship.
- Must be authorized to work in the United States for the duration of the program.
Nice To Haves
- Degree concentration in Pharmacy.
- Excellent written and verbal communication skills.
- Ability to work independently and collaboratively within cross-functional teams.
- Proficiency in Microsoft Word, PowerPoint, and Excel.
- Prior experience in clinical research through coursework, clerkships, or projects, and/or experience in clinical pharmacy.
- Familiarity with clinical trial processes or regulatory documentation.
- Strong interest in pursuing a career in the pharmaceutical or biotechnology industry.
Responsibilities
- Support clinical development of oncology compounds and day-to-day execution of clinical trials, with a focus on data quality.
- Participate in cross-functional discussions with clinical, statistics, operations, and data management teams.
- Support clinical trial operations by preparing literature reviews and slide decks and tracking study progress.
- Perform data review, identify clinical findings, and help maintain study data quality.
- Conduct background research on oncology disease states, treatments, or trial methodologies to support clinical projects.
- Assist in preparing internal presentations and literature summaries.
- Learn about the clinical scientist role in oncology clinical development through meetings, mentorship, and guided projects.
Benefits
- Competitive benefits
- Professional and personal growth and well-being support
- Networking with colleagues
- Executive and social networking events
- Community volunteer projects
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What This Job Offers
Job Type
Full-time
Career Level
Intern
