Hybrid Summer Internship: Clinical Trial Operations

Kyowa Kirin North America; Princeton (NJ); Hybrid; USD 32,000 - 45,000; Full time

Job summary

Kyowa Kirin North America invites you to join the Clinical Operations team for a paid, hybrid summer internship. You will gain hands-on exposure to how clinical studies are planned, activated, monitored, and maintained, working alongside subject-matter experts and receiving guidance from experienced Clinical Operations professionals.

The internship emphasizes document management, quality review, site support, and cross-functional collaboration, with in-office time preferred.

Qualifications

• Must be currently enrolled in a Bachelor’s, Master’s, PharmD, or PhD degree program.
• Interns must be available to work from May 25, 2027 to August 20, 2027.
• Must be eligible to work in the United States without Sponsorship.
• A minimum GPA of 3.0 is required.
• The ability to work a hybrid schedule with three days on site is required.
• Prior internship or co-op experience is preferred.
• Preferred fields of study include life sciences, health sciences, pharmaceutical sciences, healthcare administration, or a related discipline.

Responsibilities

• Contribute to clinical trial execution activities with coaching and guidance from Clinical Operations team members, including eTMF and Document Management, site management and monitoring support, and process improvement initiatives.
• Assist in monitoring trip report reviews and ensure Compliance with SOPs.
• Develop and maintain trackers and tools used by the clinical operations team, and gather information to build a comprehensive study database.
• Prepare clear and actionable department meeting minutes, capturing decisions, owners, and follow-up actions.
• Collaborate with cross-functional stakeholders to understand how Clinical Operations coordinates activities and supports timely study delivery.

Education

Bachelor’s/Master’s/PharmD/PhD program

Job description

Kyowa Kirin North America invites you to join the Clinical Operations team for a paid, hybrid summer internship. You will gain hands-on exposure to how clinical studies are planned, activated, monitored, and maintained, working alongside subject-matter experts and receiving guidance from experienced Clinical Operations professionals.

The internship emphasizes document management, quality review, site support, and cross-functional collaboration, with in-office time preferred.